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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621163Generated: October 30, 2026

Chloroacetyl chloride → HCID 178468297, compound

https://huagongshe.com/reaction/1621163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
ReactantBenzenecarboximidic acid, 3-fluoro-, ethyl ester, hydrochlorideHCID 12282165—
SolventDichloromethaneHCID 6344—
ProductHCID 178468297HCID 178468297101%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a suspension of ethyl 3-fluorobenzimidate hydrochloride (400 mg, 1.96 mmol) in dichloromethane (15 mL) was added triethylamine (497 mg, 684 μL, 4.91 mmol) at RT. The reaction mixture was cooled to 0-5° C. and 2-chloroacetyl chloride (333 mg, 234 μL, 2.95 mmol) was added dropwise over a period of 5 min. After 20 min the ice bath was removed and the mixture was stirred at RT for 2 h. The reaction mixture was poured into KHSO4 (10% aqueous solution, 25 mL) and extracted with dichloromethane (3×50 mL). The combined organic layer was dried over MgSO4 and concentrated in vacuo to give the product as light brown oil (537 mg, 1.98 mmol, 101%) which was used without further purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772510B2
Source datasetuspto-grants-2014_07
ORD IDord-f4f3a642ca4e4c9faec9dc55c7f5208c
Source noteuspto-grants-2014_07