Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910292Generated: October 27, 2026

1,4-Dibromobenzene → methyl (S)-3-(4-bromophenyl)-2-hydroxypropionate

https://huagongshe.com/reaction/910292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl (2S)-2-oxiranecarboxylateHCID 10942355—
ReactantHCID 178418260HCID 178418260—
ReactantHCID 178418306HCID 178418306—
SolventPentaneHCID 8003—
Productmethyl (S)-3-(4-bromophenyl)-2-hydroxypropionateHCID 39359925133.4%

Reaction Conditions

Temperature-30 °C

Reaction Steps

100 ml (170 mmol) of a 1.7 M solution of tert-butyllithium in pentane are added dropwise to a solution of 48 g (204 mmol) of 1,4-dibromobenzene in 160 ml of tert-butyl dimethyl ether, cooled to −30° C., followed by addition of 7.3 g (82 mmol) of copper cyanide. The reaction medium is stirred for 15 minutes and a solution of 6 ml (68 mmol) of (S)-methyl glycidate in 10 ml of tert-butyl dimethyl ether is then added. After stirring for 20 minutes at −30° C., the reaction medium is hydrolysed with 150 ml of saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with heptane, and the polarity is then increased up to a 6/4 heptane/ethyl acetate mixture. 23.5 g (44%) of methyl 3-(4-bromophenyl)-2(S)-hydroxypropanoate are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022079B2
Source datasetuspto-grants-2011_09
ORD IDord-c044be1b64664c599a14b5eb357fd1ea
Source noteuspto-grants-2011_09