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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351014Generated: October 31, 2026

N-(Diphenoxymethylene)-methanesulfonamide → N-methanesulfonyl-N'-[2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethyl]-O-phenylisourea

https://huagongshe.com/reaction/2351014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(Diphenoxymethylene)-methanesulfonamideHCID 13738851—
Reactant2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethylamineHCID 14671749—
SolventDichloromethaneHCID 6344—
ProductN-methanesulfonyl-N'-[2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethyl]-O-phenylisoureaHCID 1984790178%

Reaction Steps

11.6 g of diphenyl methanesulfonylimidocarbonate was dissolved in 40 ml of methylene chloride. With ice-cooling, thereto was added 15 g of 2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethylamine. The mixture was stirred for 10 minutes. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by a column chromatography (eluant: benzene:ethyl acetate=2:1) to obtain 17.8 g (yield: 78%) of oily N-methanesulfonyl-N'-[2-[[5-[N-methyl-N-(2,2,2-trichloroethoxycarbonyl)aminomethyl]-2furyl]methylthio]ethyl]-O-phenylisourea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871765
Source datasetuspto-grants-1989_10
ORD IDord-e0e9d4ffb1b143bd82890815b91456a9
Source noteuspto-grants-1989_10