HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111363Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 3076390, compound
https://huagongshe.com/reaction/1111363
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 3076416 | HCID 3076416 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 3076390 | HCID 3076390 | 52.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04980356 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-8e4a3d4d88bc4b4c8fb597ad1e39d264 |
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| Source note | uspto-grants-1990_12 |
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