tert-Butyl 4-hydroxybutyrate

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Company Name: Shaanxi Yikunte Pharmaceutical Technology Co., Ltd.  Gold
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Company Name: Wuhan EEChem Technologies Co., Ltd  Gold
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tert-Butyl 4-hydroxybutyrate manufacturers

tert-Butyl 4-hydroxybutyrate Basic information
Product Name:tert-Butyl 4-hydroxybutyrate
Synonyms:2-(2-hydroxyethyl)-3,3-dimethylbutanoate;Butanoic acid, 4-hydroxy-, 1,1-diMethylethyl ester;4-Hydroxy-butyric acid tert-butyl ester;tert-butyl 4-hydroxybutanoate - [B87055];tert-butyl 4-hydroxybutanoate
CAS:59854-12-5
MF:C8H16O3
MW:160.21
EINECS:
Product Categories:
Mol File:59854-12-5.mol
tert-Butyl 4-hydroxybutyrate Structure
tert-Butyl 4-hydroxybutyrate Chemical Properties
Boiling point 73-74 °C(Press: 2.0-3.0 Torr)
density 0.976 g/mL at 20 °C
refractive index n20/D 1.431
Fp >70℃
storage temp. Refrigerator
solubility Chloroform (Slightly), Methanol (Slightly), Water (Slightly)
form Oil
pka14.86±0.10(Predicted)
color Colourless to Pale Yellow
InChIInChI=1S/C8H16O3/c1-8(2,3)11-7(10)5-4-6-9/h9H,4-6H2,1-3H3
InChIKeyRXGFTUPFXKYRMW-UHFFFAOYSA-N
SMILESC(OC(C)(C)C)(=O)CCCO
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
HS Code 2915601990
MSDS Information
tert-Butyl 4-hydroxybutyrate Usage And Synthesis
Usestert-Butyl 4-Hydroxybutanoate is used as a reagent in the synthesis of theranostic vitamin-linker-taxoid conjugates. tert-Butyl 4-Hydroxybutanoate is also used as a reagent in the synthesis of teroxazoles as α-helix mimetics.
Synthesis
Mono-tert-butyl succinate

15026-17-2

TERT-BUTYL 4-HYDROXYBUTYRATE

59854-12-5

General procedure for the synthesis of tert-butyl 4-hydroxybutyrate from mono-tert-butyl succinate: BH3-Me2S (2.0 M solution in THF, 6.6 mL, 13.1 mmol) was slowly added dropwise to a solution of mono-tert-butyl succinate (2.12 g, 12.2 mmol) in anhydrous THF (20 mL) that was cooled to 0 °C. The reaction mixture was gradually warmed to room temperature and stirred continuously for 24 hours. Upon completion of the reaction, EtOAc (100 mL) was added for dilution and the organic layer was separated. The organic layer was washed sequentially with water (70 mL) and saturated saline (70 mL) and dried with anhydrous MgSO4. After filtration, the solvent was removed by concentration under reduced pressure to afford tert-butyl 4-hydroxybutyrate (1.92 g, 12.2 mmol, quantitative yield), the product was a light yellow oil, which could be used in the subsequent reaction without further purification.

References[1] Tetrahedron, 2014, vol. 70, # 44, p. 8343 - 8347
[2] Bioconjugate Chemistry, 2010, vol. 21, # 5, p. 979 - 987
[3] Beilstein Journal of Organic Chemistry, 2017, vol. 13, p. 2428 - 2441
[4] Journal of Organic Chemistry, 2003, vol. 68, # 17, p. 6679 - 6684
[5] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 18, p. 4004 - 4009
Tag:tert-Butyl 4-hydroxybutyrate(59854-12-5) Related Product Information
Z-Asp(OtBu)-OH dcha H-Asp(OtBu)-OtBu HCl Dihydrocytochalasin B N-Cbz-L-Aspartic acid 4-tert-butyl ester Boc-Asp-OtBu D-Aspartic acid 4-tert-butyl ester Boc-L-aspartic acid 4-tert-butyl ester Fmoc-D-Aspartic acid beta-tert-butyl ester Fmoc-Asp(OtBu)-OH L-Fmoc-Aspartic acid alpha-tert-butyl ester 4-tert-Butyl N-[(tert-butoxy)carbonyl]-L-aspartate dicyclohexylamine salt L-Aspartic acid 4-tert-butyl ester Boc-Asp(OtBu)-OSu Fmoc-Asp(OtBu)-OPfp N-alpha-Benzyloxycarbonyl-L-aspartic acid alpha-tert-butyl ester dicyclohexylamine Boc-D-Asp(OtBu)-OH dcha Boc-Asp(OtBu)-ONp L-Aspartic acid di-tert-butyl ester dibenzenesulfimide salt