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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111363Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 3076390, compound

https://huagongshe.com/reaction/1111363

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 3076416HCID 3076416—
SolventEthanolHCID 702—
ProductHCID 3076390HCID 307639052.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

m-Chloroperbenzoic acid (0.6 g) is added in the course of approximately 10 minutes to 2-imino-3-(2-phenylthioethyl)-6-trifluoromethoxybenzothiazoline (1.3 g) in absolute ethanol (20 cc) cooled to 0° C. The reaction is continued for 3 hours at a temperature in the region of 20° C. The reaction medium is concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) and the residue obtained purified by chromatography on a silica column with ethyl acetate as eluent. (RS)-2-Imino-3-(2-phenylsulphinylethyl)-6-trifluoromethoxybenzothiazoline (0.7 g) is obtained in the form of a yellowish oil, which is converted to a hydrochloride, m.p. 210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980356
Source datasetuspto-grants-1990_12
ORD IDord-8e4a3d4d88bc4b4c8fb597ad1e39d264
Source noteuspto-grants-1990_12