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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748146Generated: October 30, 2026

Chloroacetyl chloride → HCID 58040950, compound

https://huagongshe.com/reaction/1748146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
ReactantS-TritylcysteamineHCID 262764—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 58040950HCID 5804095086.6%

Reaction Steps

Dissolve 2-[(triphenylmethyl)thio]ethylamine (5.24 g, 16.4 mmol) and triethylamine (2.76 mL, 19.6 mmol) in 150 mL dichloromethane. Chloroacetyl chloride (1.56 mL, 19.6 mmol) is dissolved in 20 mL chloroform. Being cooled down with an ice bath, slowly drop chloroacetyl chloride into the solution. Then stir the solution at room temperature for 2 hours. Next wash organic phase with followings in turn: 2N hydrochloric acid solution (120 mL), and saturated sodium bicarbonate aqueous solution (100 mL). The organic phase is dehydrated by anhydrous sodium sulfate (Na2SO4) and then is concentrated in vacuo to yield yellow oily N-[2-((Triphenylmethyl)thio) ethyl]-chloroacetamide (5.62 g, 86.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150602B2
Source datasetuspto-grants-2015_10
ORD IDord-511611c65bcc48019eb6b00a3d7edc80
Source noteuspto-grants-2015_10