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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607102Generated: October 27, 2026

Methyl Isocyanate → N-triphenylmethyl-2-methylaminocarbonylthioethylamine

https://huagongshe.com/reaction/1607102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
ReactantN-triphenylmethylcysteamineHCID 15616512—
SolventDichloromethaneHCID 6344—
ProductN-triphenylmethyl-2-methylaminocarbonylthioethylamineHCID 1561651479%

Reaction Steps

Methylisocyanate (243 mg) was dissolved in anhydrous dichloromethane (5 ml). To the solution were added N-triphenylmethylcysteamine (3.19 g: 0.33 equimolar amount) while cooling with ice. The reaction solution was stirred at room temperature for 4 hours and was concentrated under reduced pressure. The residue was dissolved in chloroform (50 ml), and the chloroform solution was well washed with water and a saturated solution of sodium chloride. Anhydrous sodium sulate was used to dry the chloroform layer which was then concentrated under reduced pressure. The residue was purified by silica gel chromatography using a solvent system of hexane/ethyl acetate (5:1 v/v) to obtain the desired substance (297 mg) with a yield of 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863935
Source datasetuspto-grants-1989_09
ORD IDord-88a1850dfd1e43d28f014436e301362c
Source noteuspto-grants-1989_09