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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940884Generated: October 27, 2026

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

https://huagongshe.com/reaction/1940884

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 mils 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 numberUS05700945
Source datasetuspto-grants-1997_12
ORD IDord-0f8cf330da5c401ca6ca0ca586526216
Source noteuspto-grants-1997_12