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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470945Generated: October 30, 2026

Ethanol → 7-(2-Chloroacetyl)-4-hydroxybenzo[d]thiazol-2(3H)-one

https://huagongshe.com/reaction/470945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant7-Acetyl-4-hydroxybenzo[d]thiazol-2(3H)-oneHCID 45076987—
ReactantTrimethylbenzylammonium DichloroiodateHCID 56924451—
SolventWaterHCID 962—
Product7-(2-Chloroacetyl)-4-hydroxybenzo[d]thiazol-2(3H)-oneHCID 57989327—

Reaction Conditions

Temperature78 °C

Reaction Steps

Ethanol (1500 mL) was added to a mixture of 7-acetyl-4-hydroxy-3H-benzothiazol-2-one (150 g) (WO2004/016578) and benzyltrimethylammonium dichloroiodate (374 g) in a flask fitted with an overhead stirrer. The mixture was heated to 78° C. for 1 h and left to cool to room temperature overnight. The mixture was poured into water (2 L), and the precipitate collected by filtration, washed with water, filtered to near dryness, and suspended in ethyl acetate. The mixture was heated to reflux and allowed to cool to room temperature with stirring. The solid was collected by filtration, washed with cold ethyl acetate (200 mL) then re-suspended in diethyl ether (1 L). The solid was collected, filtered again and washed with ether (200 mL) and dried in vacuo to give the subtitled compound. Yield 164 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629271B2
Source datasetuspto-grants-2014_01
ORD IDord-77c93e6acbda4e77a7e0ea44030958e6
Source noteuspto-grants-2014_01