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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736658Generated: October 27, 2026

1,3-Dichloroacetone → 2-Acetoxymethyl-4-chloromethyl-4-hydroxythiazoline

https://huagongshe.com/reaction/1736658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantSodium BicarbonateHCID 516892—
ReactantCarbamothioylmethyl acetateHCID 11018908—
Solvent1,2-DichloroethaneHCID 11—
Product2-Acetoxymethyl-4-chloromethyl-4-hydroxythiazolineHCID 1179082792%

Reaction Steps

A mixture of 5.33 g of 2-acetoxythioacetamide prepared according to Example 2, 5.21 g of 1,3-dichloroacetone, 6.88 g of sodium bicarbonate and 20 ml of 1,2-dichloroethane was stirred at room temperature for 87 hours. The mixture was filtered to remove insoluble inorganics and concentrated under reduced pressure to an oil. The oil was taken up in 4 mls of 1,2-dichloroethane and 25 mls of cyclohexane added dropwise. The slurry was stirred for 1 hour at 0° C. and then filtered. The precipitate was washed with cyclohexane and dried at room temperature under reduced pressure. The product, 2-acetoxymethyl-4-chloromethyl-4-hydroxy-thiazoline was obtained in 92% yield (8.25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541335
Source datasetuspto-grants-1996_07
ORD IDord-84a7b57dc03e4b0593f80a82f4ebdeea
Source noteuspto-grants-1996_07