HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255456Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 15165517, compound
https://huagongshe.com/reaction/2255456
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2(3H)-Benzothiazolimine, 3-[3-(methylthio)propyl]-6-(trifluoromethoxy)- | HCID 10543830 | — |
| Reactant | HCID 86747166 | HCID 86747166 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15165517 | HCID 15165517 | — |
Reaction Steps
2-(3-Chlorobenzoylimino)-3-(3-methyl-sulphonylpropyl)-6-trifluoromethoxybenzothiazoline may be prepared in the following way: 75% m-chloro-perbenzoic acid (5.2 g) is added in the course of about 10 minutes, to 2-imino-3-(3-methylthiopropyl)-6-trifluoromethoxybenzothiazoline (3.9 g) in solution in dichloromethane (100 cc) stirred at a temperature close to 20° C. The reaction mixture is brought to the boil for 18 hours. After cooling to a temperature close to 20° C., the precipitate is filtered off and washed with dichloromethane (50 cc) and the filtrate is concentrated to dryness under reduced pressure after washing with 1N sodium hydroxide solution. The oil obtained is crystallised from ethyl acetate. 2-(3-Chlorobenzoylimino)-3-(3-methylsulphonylpropyl)-6-trifluoromethoxybenzothiazoline (0.6 g) melting at 188° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05240948 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-a5209cc5b8d843d1aa5bafde76a3176a |
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| Source note | uspto-grants-1993_08 |
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