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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429787Generated: October 25, 2026

Chloroacetyl chloride → 1-(Chloroacetyl)pyrrolidine

https://huagongshe.com/reaction/429787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium HydroxideHCID 14798—
ReactantPyrrolidineHCID 31268—
Reactant4,5-DimethylthiazoleHCID 62510—
Reactant1-(Chloroacetyl)pyrrolidineHCID 88440—
SolventDichloromethaneHCID 6344—
Product1-(Chloroacetyl)pyrrolidineHCID 88440—
Product3-(2-(1-Pyrrolidinyl)-2-oxoethyl)-4,5-dimethyl-thiazolium chlorideHCID 9943136—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(2-(1-pyrrolidinyl)-2-oxoethyl)-4,5-dimethyl-thiazolium chloride was prepared from the reaction of N-(chloroacetyl)pyrrolidine with 4,5-dimethylthiazole. N-(chloroacetyl)pyrrolidine was prepared as follows. Pyrrolidine (63.9 g, 0.9 mol) was taken in methylene chloride (640 mL) and cooled to 0° C. in a salt-ice bath. To the stirred mixture was added chloroacetyl chloride (101.8 g in 450 mL of CH2, Cl2, 0.9 mol) dropwise keeping the inside temperature below 15° C. After adding the chloroacetyl chloride, the mixture was stirred for an hour at 5° C. Sodium hydroxide solution (7 M, 190 mL) was added with vigorous stirring such that the inside temperature did not exceed 20° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319934B1
Source datasetuspto-grants-2001_11
ORD IDord-ffc88bb2f5944b068e9fb000009b0ac5
Source noteuspto-grants-2001_11