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3-BROMOPHENETOLE

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3-BROMOPHENETOLE Basic information
Product Name:3-BROMOPHENETOLE
Synonyms:M-BROMOPHENETOLE;3-ETHOXYBROMOBENZENE;3-BROMOPHENETOLE;3-BROMOPHENYL ETHYL ETHER;AKOS 314;3-Bromophenetol;3-Bromophenetole,3-Bromophenyl ethyl ether;3-broMoethoxybenzene
CAS:2655-84-7
MF:C8H9BrO
MW:201.06
EINECS:220-186-9
Product Categories:Phenetole;Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds;alkyl bromide
Mol File:2655-84-7.mol
3-BROMOPHENETOLE Structure
3-BROMOPHENETOLE Chemical Properties
Boiling point 206 °C (lit.)
density 1.481 g/mL at 25 °C (lit.)
refractive index n20/D 1.548(lit.)
Fp 182 °F
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light yellow to Light orange
Specific Gravity1.481
InChI1S/C8H9BrO/c1-2-10-8-5-3-4-7(9)6-8/h3-6H,2H2,1H3
InChIKeyLQBMPJSTUHWGDE-UHFFFAOYSA-N
SMILESCCOc1cccc(Br)c1
CAS DataBase Reference2655-84-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
WGK Germany 3
HS Code 2909309090
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
3-BROMOPHENETOLE Usage And Synthesis
Synthesis
3-Bromophenol

591-20-8

Iodoethane

75-03-6

3-BROMOPHENETOLE

2655-84-7

General procedure for the synthesis of 3-ethoxybromobenzene: Sodium hydride (18.4 g, 60% oil dispersion, 460 mmol) was suspended in 1000 mL of DMF and the mixture was cooled to 0 °C. 3-Bromophenol (72 g, 419 mmol) was placed in a dropping funnel and heated using a hot air gun to melt it and then added dropwise to the cooled sodium hydride suspension. After the dropwise addition, the reaction mixture was continued to be stirred at 0 °C for 30 min. Subsequently, iodoethane (40 mL, 78 g, 503 mmol) was slowly added dropwise and the mixture was stirred for 12 hours, during which time it was allowed to warm naturally to room temperature. Upon completion of the reaction, water (1000 mL) was carefully added to quench the reaction, followed by extraction with ethyl acetate (4 x 500 mL). The organic layers were combined, washed with water (8 x 200 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The residue was distilled under reduced pressure and the fractions with boiling points above 120 °C were collected to give 70 g of the target product 3-ethoxybromobenzene in 84% yield. The density of the product was 1.47 g/mL.

References[1] Patent: US5914329, 1999, A
[2] Patent: EP944611, 2004, B1. Location in patent: Page 6-7
[3] Patent: US2018/290997, 2018, A1. Location in patent: Paragraph 0209
3-BROMOPHENETOLE Preparation Products And Raw materials
Raw materials3-Bromophenol-->Iodoethane-->Sodium hydride-->N,N-Dimethylformamide
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