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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221688Generated: October 31, 2026

Methanol → N-[1-(3-Bromo-phenyl)-2,2-difluoro-1-hydroxymethyl-ethyl]-2-chloro-acetamide

https://huagongshe.com/reaction/221688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-2-(3-bromo-phenyl)-3,3-difluoro-propan-1-ol hydrochlorideHCID 66665881—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solventtert-Butyl methyl etherHCID 15413—
ProductN-[1-(3-Bromo-phenyl)-2,2-difluoro-1-hydroxymethyl-ethyl]-2-chloro-acetamideHCID 66665688—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Amino-2-(3-bromo-phenyl)-3,3-difluoro-propan-1-ol hydrochloride (6.5 g, 24.43 mmol) was put between 60 ml aqueous 2 M Na2CO3 solution and 60 ml dichloromethane and cooled to 0° C. under strong stirring. Then chloroacetylchloride (2.94 ml, 36.6 mmol), diluted in 8 ml dichloromethane, was added dropwise to the biphasic solution. After the complete addition, the reaction was stirred for 30 minutes at r.t. After completion 10 ml MeOH were added and stirring was continued for 10 minutes. Then TBME and water were added. The phases were separated, and the aqueous phase was extracted with TBME. The organic phases were washed with water and brine, dried over Na2SO4 and concentrated under reduced pressure to yield the title compound as off-white solid. 1H-NMR (360 MHz, DMSO-d6): 8.72 (s, 1H), 7.53 (m, 2H), 7.35 (m, 2H), 6.48 (t, 1H, CHF2), 5.39 (t, 1H), 4.18 (m, 2H), 3.10 (s, 2H); MS: 342 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207164B2
Source datasetuspto-grants-2012_06
ORD IDord-962e981bdfec4b11968e1cef679103fa
Source noteuspto-grants-2012_06