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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255456Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 15165517, compound

https://huagongshe.com/reaction/2255456

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2(3H)-Benzothiazolimine, 3-[3-(methylthio)propyl]-6-(trifluoromethoxy)-HCID 10543830—
ReactantHCID 86747166HCID 86747166—
SolventDichloromethaneHCID 6344—
ProductHCID 15165517HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240948
Source datasetuspto-grants-1993_08
ORD IDord-a5209cc5b8d843d1aa5bafde76a3176a
Source noteuspto-grants-1993_08