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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445761Generated: November 2, 2026

Acetone → 4-Benzyloxy-2-(4-bromo-2-fluoro-benzoylamino)-butyric acid

https://huagongshe.com/reaction/1445761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2-fluorobenzoyl chlorideHCID 2734026—
Reactant2-Amino-4-(benzyloxy)butanoic acid hydrochlorideHCID 68698920—
SolventPropan-2-one--water (1/1)HCID 18366337—
Product4-Benzyloxy-2-(4-bromo-2-fluoro-benzoylamino)-butyric acidHCID 58951433—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of 2-amino-4-benzyloxy-butyric acid hydrochloride salt (1.0 mmol) (See Intermediate 34) and sodium carbonate (3.0 mmol) in 1:1 acetone/water (0.5M) in a 0° C. ice bath, slowly add 4-bromo-2-fluoro-benzoyl chloride (1.2 mmol) diluted in acetone (prepared from 4-bromo-2-fluoro-benzoic acid (1.0 mmol) and oxalyl chloride (1.0 mmol) in dichloromethane using catalytic dimethylformamide). Stir for 30 minutes at 0° C. After this time, wash the reaction with 1N hydrochloric acid while extracting with ethyl acetate. Concentrate the organics in vacuo. Purify on an Isco CombiFlash® chromatography system eluting with 1% acetic acid in ethyl acetate and hexane. MS (m/e) (79Br/81Br): 410.3/412.3 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666871B2
Source datasetuspto-grants-2010_02
ORD IDord-abf392cb93b945ac93ee06688db8ca0d
Source noteuspto-grants-2010_02