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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276395Generated: October 26, 2026

2-Methyl-4-nitrophenyl isothiocyanate → 2-(2-Methyl-4-nitrophenylimino)-3-(1-cyclohexyl-1-ethyl)-1,3-thiazolidine

https://huagongshe.com/reaction/276395

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-nitrophenyl isothiocyanateHCID 145621—
ReactantN-(2-chloroethyl)-N-(1-cyclohexyl-1-ethyl)ammonium chlorideHCID 18316241—
Product2-(2-Methyl-4-nitrophenylimino)-3-(1-cyclohexyl-1-ethyl)-1,3-thiazolidineHCID 18316295—

Reaction Steps

1-Cyclohexyl-1-ethylamine was converted to N-(2-hydroxyethyl)-N-(1-cyclohexyl-1-ethyl)amine according to Method B5a. The alcohol was reacted with SOCl2 according to Method B7a to give N-(2-chloroethyl)-N-(1-cyclohexyl -1-ethyl)ammonium chloride. The chloroethylamine was reacted with 2-methyl-4-nitrophenyl isothiocyanate according to Method C1a to give 2-(2-methyl-4-nitrophenylimino)-3-(1-cyclohexyl-1-ethyl)-1,3-thiazolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353006B1
Source datasetuspto-grants-2002_03
ORD IDord-86c9079b29274ce39c465557da60751e
Source noteuspto-grants-2002_03