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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885561Generated: November 3, 2026

Hydrogen Sulfide → tert-butyl N-(1-carbamothioyl-1-methylethyl)carbamate

https://huagongshe.com/reaction/1885561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantTriethylamineHCID 8471—
Reactanttert-butyl N-(1-cyano-1-methylethyl)carbamateHCID 18316698—
SolventBenzeneHCID 241—
Producttert-butyl N-(1-carbamothioyl-1-methylethyl)carbamateHCID 15186362—

Reaction Steps

2-tert-Butyloxycarbonylamino-2-methylpropiononitrile (80.00 g) in Benzene (700 ml) was stirred at 0° C., and saturated with hydrogen sulfide. To the reaction mixture was dropped triethyl amine (1000 ml) and bubbled hydrogen sulfide at ambient temperature for 9 hours, and left at the same temperature for 19 hours. The reaction mixture was added to water and extracted with ethyl acetate. The organic layer was washed with water, saturated aqueous sodium hydrogencarbonate, water and brine, and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo. The residue was washed with n-hexane, to give 2-tert-butyloxycarbonylamino-2-methylpropanethioamide (80.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05145860
Source datasetuspto-grants-1992_09
ORD IDord-802ac01fc5ce4b3da4abc8b1805351e8
Source noteuspto-grants-1992_09