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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216176Generated: October 26, 2026

Methyl iodide → 2-(3-Bromophenyl)propanoic acid

https://huagongshe.com/reaction/216176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant(3-Bromophenyl)acetic acidHCID 74653—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Bromophenyl)propanoic acidHCID 12797954100%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of LDA in THF/n-heptane/ethylbenzene (1.8M, 23.25 mL, 41.85 mmol) is cooled down to −78° C. and added a solution of 3-bromophenylacetic acid [3 g, 13.95 mmol, Intermediate (68)] in THF (7 mL) dropwise over 15 minutes. The mixture is stirred for 1 h at −78° C. and treated dropwise with methyl iodide (6.34 g, 44.64 mmol) over 15 minutes. The reaction mixture is warmed up to room temperature and after stirring overnight, the mixture is quenched with 2N hydrochloric acid and concentrated to remove THF. The residue is diluted with ether, washed twice with 2 N hydrochloric acid (20 mL) and extracted twice with 10% sodium hydroxide (20 mL). The combined sodium hydroxide extracts are acidified with 6 N hydrochloric acid to pH=1 and extracted three times with ether (50 mL). Combined organic extracts are washed with brine, dried over sodium sulfate and concentrated to obtain 2-(3-bromo-phenyl)-propionic acid [3 g, 100%, Intermediate (69)] as a solid, which is used without further purification. LC/MS: 229 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193183B2
Source datasetuspto-grants-2012_06
ORD IDord-a261cc4345474c57aa167b3464509409
Source noteuspto-grants-2012_06