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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81607Generated: October 30, 2026

Chloroacetyl chloride → N-(2-(5-bromo-2-fluorophenyl)-3,3-difluoro-4-hydroxybutan-2-yl)-2-chloroacetamide

https://huagongshe.com/reaction/81607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66666062HCID 66666062—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductN-(2-(5-bromo-2-fluorophenyl)-3,3-difluoro-4-hydroxybutan-2-yl)-2-chloroacetamideHCID 66665738—

Reaction Steps

To an ice cooled solution of 3-amino-3-(5-bromo-2-fluorophenyl)-2,2-difluorobutan-1-ol (3.1 g, 10.4 mmol), in DCM (60 ml) was added aqueous Na2CO3 (2.74 g, 25.8 mmol in 7.0 mL H2O) and stirred for 10 min. Chloroacetyl chloride (0.986 ml, 11.4 mmol) was then added to the resultant reaction mixture and stirring continued for 30 min at 0° C. Upon formation of the new product by TLC analysis, K2CO3 (1.5 g, 10.4 mmol) in MeOH (17 mL) was added to the reaction mixture and stirred at rt for 30 min. The reaction mixture was diluted with DCM, separated the organic layer and washed successively with water and brine solution, dried over anhydrous Na2SO4 and concentrated under reduced pressure to furnish title compound as a colorless gum. Yield=3.3 g (78.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846658B2
Source datasetuspto-grants-2014_09
ORD IDord-ab319730f57d4eb7a5d06b517f7bb411
Source noteuspto-grants-2014_09