ChemicalBook >> CAS DataBase List >>Ethyl (trimethylsilyl)acetate

Ethyl (trimethylsilyl)acetate

CAS No.
4071-88-9
Chemical Name:
Ethyl (trimethylsilyl)acetate
Synonyms
ETSA;2-trimethylsilylbutanoate;Ethyl(Trimethylsily)Acetate;ETHYL (TRIMETHYLSILYL)ACETATE;ETHYL(2-TRIMETHYLSILYL)ACETATE;ETHYL TRI METHYLSILYLACETATE 99%;Ethyl (trimethylsilyl)acetate,97%;Ethyl acetatethree Methylsilicone;Ethyl (trimethylsilyl)acetate, 98+%;(TRIMETHYLSILYL)ACETIC ACID ETHYL ESTER
CBNumber:
CB7271085
Molecular Formula:
C7H16O2Si
Molecular Weight:
160.29
MDL Number:
MFCD00009172
MOL File:
4071-88-9.mol
MSDS File:
SDS
Last updated:2026-05-28 05:47:38
Product description Number Pack Size Price
Ethyl trimethylsilylacetate ≥98% 209120 25g $244
Ethyl (Trimethylsilyl)acetate >93.0%(GC) T1584 5g $46
Ethyl (Trimethylsilyl)acetate >93.0%(GC) T1584 25g $138
Ethyl (Trimethylsilyl)acetate Asreported 275985 5g $325
Ethyl (Trimethylsilyl)acetate Asreported 275985 10g $452
More product size

Ethyl (trimethylsilyl)acetate Properties

Boiling point 156-159 °C (lit.)
Density 0.876 g/mL at 25 °C (lit.)
refractive index n20/D 1.415(lit.)
Flash point 95 °F
storage temp. Inert atmosphere,Room Temperature
solubility sol ethereal and chlorinated solvents; reacts with protic solvents.
form clear liquid
color Colorless to Almost colorless
Specific Gravity 0.876
Water Solubility Decomposition
Hydrolytic Sensitivity 2: reacts with aqueous acid
Sensitive Moisture Sensitive
BRN 1755902
InChI 1S/C7H16O2Si/c1-5-9-7(8)6-10(2,3)4/h5-6H2,1-4H3
InChIKey QQFBQBDINHJDMN-UHFFFAOYSA-N
SMILES CCOC(=O)C[Si](C)(C)C
CAS DataBase Reference 4071-88-9(CAS DataBase Reference)
FDA UNII JJ5WZD3DYT
NIST Chemistry Reference Ethyl (trimethylsilyl)acetate(4071-88-9)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)
GHS02
Signal word  Warning
Hazard statements  H226
Precautionary statements  P210-P240-P241-P280a-P303+P361+P353-P501a
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Risk Statements  10
Safety Statements  16-24/25
RIDADR  UN 3272 3/PG 3
WGK Germany  3
10-21
TSCA  Yes
HazardClass  3
PackingGroup  III
HS Code  29319090
Storage Class 3 - Flammable liquids
Hazard Classifications Flam. Liq. 2
NFPA 704
3
0 0

Ethyl (trimethylsilyl)acetate price More Price(48)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 209120 Ethyl trimethylsilylacetate ≥98% 4071-88-9 25g $244 2022-05-15 Buy
TCI Chemical T1584 Ethyl (Trimethylsilyl)acetate >93.0%(GC) 4071-88-9 5g $46 2026-04-30 Buy
TCI Chemical T1584 Ethyl (Trimethylsilyl)acetate >93.0%(GC) 4071-88-9 25g $138 2026-04-30 Buy
Usbiological 275985 Ethyl (Trimethylsilyl)acetate Asreported 4071-88-9 5g $325 2026-06-03 Buy
Usbiological 275985 Ethyl (Trimethylsilyl)acetate Asreported 4071-88-9 10g $452 2026-06-03 Buy
Product number Packaging Price Buy
209120 25g $244 Buy
T1584 5g $46 Buy
T1584 25g $138 Buy
275985 5g $325 Buy
275985 10g $452 Buy

Ethyl (trimethylsilyl)acetate Chemical Properties,Uses,Production

Chemical Properties

Ethyl trimethylsilylacetate is a clear colorless liquid. It is stable to the usual manipulations, and can be stored in glass containers for years without change of physical and spectral properties.

Uses

(silylating agent; source of an ethyl acetate anion equivalent.Ethyl trimethylsilylacetate is reactive to nucleophiles and readily undergoes desilylation reactions with acid or alkali,ethanol, and bromine.
Ethyl (trimethylsilyl)acetate Reaction

Uses

Ethyl trimethylsilylacetate is used in the synthesis of ethyl-2,2-dibromo-2-(trimethylsilyl)acetate and α,β-unsaturated esters. It was also used to silylate the enolizable aldehydes and ketones.

Preparation

ethyl trimethylsilylacetate synthesis: Available by a Reformatsky reaction from ethyl bromoacetate, and by reaction of trimethylsilylmethylmagnesium chloride with ethyl chloroformate. An alternative approach requires the treatment of ethyl acetate with triphenylmethylsodium followed by chlorotrimethylsilane The use of a nitrogen base with ethyl acetate in THF followed by reaction with chlorotrimethylsilane results in a mixture of C- and O-silylation. The use of HMPA as additive in the reaction medium increases the amount of O-silylation to 90%. Similar methods can be used to prepare analogs.

General Description

Reaction of ethyl trimethylsilylacetate (ETSA) with dilute hydrochloric acid, dilute alkali, anhydrous HCl, anhydrous bromine and absolute ethanol has been reported. ETSA undergoes condensation with aromatic aldehydes in the presence of base catalyst to yield β-trimethylsiloxycarboxylates. Lithium ETSA reacts with ketones to yield α,β-unsaturated esters.

Synthesis

Ethyl bromoacetate

105-36-2

Ethyl (trimethylsilyl)acetate

4071-88-9

Zinc powder (9.92 g, 152 mmol) and copper(I) chloride (1.50 g, 15.2 mmol) were added to 15 mL of dry benzene under nitrogen protection, stirred and refluxed for 30 min. Subsequently, trimethylchlorosilane (12.8 mL, 101 mmol) and ethyl bromoacetate (12.3 mL, 111 mmol) dissolved in a mixture of 23 mL of anhydrous tetrahydrofuran and 21 mL of anhydrous benzene were slowly added through a dropping funnel, maintaining a mild reflux condition. The titration process took about 1 hour. After dropwise addition, reflux was continued for 1 hour, followed by cooling in an ice bath. Under stirring, 30 mL of 5% aqueous hydrochloric acid solution was added through a dropping funnel in 10 minutes. The liquid layer was separated and the reaction flask was washed with ether. The organic phase was combined and washed sequentially with saturated sodium bicarbonate solution twice, saturated sodium chloride solution twice, then saturated sodium bicarbonate solution twice, and finally saturated sodium chloride solution twice. The combined organic layers were dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the crude product. Purification by reduced pressure distillation (boiling point 93-94 °C, 104 mmHg) gave ethyl 2-(trimethylsilyl)acetate as a pale yellow liquid in 74% yield (12.0 g, 74.9 mmol).1H NMR (CDCl3) δ 4.09 (q, J = 7.1 Hz, 2H), 1.89 (s, 2H), 1.24 (t, J = 7.1 Hz. 3H), 0.12 (s, 9H).

Purification Methods

Purify it by distilling ca 10g of reagent through a 15cm, Vigreux column (p 11) and then redistilling it through a 21cm glass helices-packed column [Hauze & Hauser J Am Chem Soc 75 994 1953]. Alternatively, dissolve it in Et2O, wash with H2O, dilute Na2CO3, dry over Na2CO3, evaporate Et2O, and distil it through a column of 15 theoretical plates. [Gold et al. J Am Chem Soc 70 2874 1948, Beilstein 4 IV 3974.]

References

[1] Chemistry Letters, 2017, vol. 46, # 2, p. 228 - 231

Global( 206)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 +86-18192627656 1059@dideu.com China 3703 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29640 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-2158073036 info@dakenam.com China 14014 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21586 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
HaBo Hong Kong Co., Limited.
+86-25-18512596065 info@habotech.com CHINA 933 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19936 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58

View Lastest Price from Ethyl (trimethylsilyl)acetate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ethyl (trimethylsilyl)acetate pictures 2025-12-12 Ethyl (trimethylsilyl)acetate
4071-88-9
$20.00-30.00 1KG 99% 200000KG Shaanxi Dideu Medichem Co. Ltd
Ethyl (trimethylsilyl)acetate pictures 2019-12-23 Ethyl (trimethylsilyl)acetate
4071-88-9
$1.00 1g 99% 1000KGS Career Henan Chemical Co
ETHYL 2-(TRIMETHYLSILYL)ACETATE, 97%ETHYL 2-(TRIMETHYLSILYL)ACETATE, 97%ETHYL 2-(TRIMETHYLSILYL)ACETATE, 97% ETHYL(2-TRIMETHYLSILYL)ACETATE ETHYL (TRIMETHYLSILYL)ACETATE ETSA (TRIMETHYLSILYL)ACETIC ACID ETHYL ESTER ETHYL TRI METHYLSILYLACETATE 99% Ethyl(Trimethylsily)Acetate ETSA~(Trimethylsilyl)acetic acid ethyl ester 2-trimethylsilylbutanoate Ethyl (trimethylsilyl)acetate, 98+% 2-(Trimethylsilyl)acetic acid ethyl ester 2-[Dimethyl(methyl)silyl]acetic acid ethyl ester Ethyl (trimethylsilyl)acetate,97% (Trimethylsilyl)acetic Acid Ethyl Ester ETSA Ethyl acetatethree Methylsilicone Acetic acid, (trimethylsilyl)-, ethyl ester TIANFUCHEM-- 4071-88-9--Ethyl (trimethylsilyl)acetate in stock 4071-88-9 C7H16O2Si CH33SiCH2CO2CH2CH3 CH33SiCH2CO2C2H5 Carbonyl Compounds C6 to C7 Building Blocks Si (Classes of Silicon Compounds) Silicon Compounds (for Synthesis) Si-(C)4 Compounds Organic Building Blocks Esters Si (Classes of Silicon Compounds) Si-(C)4 Compounds Silicon Compounds (for Synthesis) Synthetic Organic Chemistry