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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482215Generated: October 31, 2026

tert-Butyl mercaptan → Tert-butyl (2-(tert-butyldisulfanyl)ethyl)carbamate

https://huagongshe.com/reaction/1482215

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl mercaptanHCID 6387—
Reactant1-ChlorobenzotriazoleHCID 88761—
ReactantThioureaHCID 2723790—
ReactantN-(tert-butoxycarbonyl)-2-aminoethanethiolHCID 3017761—
ReactantHCID 178418385HCID 178418385—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl (2-(tert-butyldisulfanyl)ethyl)carbamateHCID 8966830877%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1-Chloro-1H-benzo[d][1,2,3]triazole (1.73 g, 11.28 mmol) and 1H-benzo[d][1,2,3]triazole (0.67 g, 5.64 mmol) were dissolved in DCM (24.0 ml) under a nitrogen atmosphere, the mixture was cooled to −78° C., and a solution of tert-butyl(2-mercaptoethyl)carbamate (Compound 6a) (1.00 g, 5.64 mmol) in DCM (3.0 ml) was added dropwise. Following stirring at 78° C. for 10 minutes, a suspension of thiourea (1.29 g, 16.92 mmol) in THF (6.0 ml) was added and the mixture was further stirred for 10 minutes. A solution of 2-methylpropane-2-thiol (0.76 g, 8.46 mmol) in DCM (3.0 ml) was then added dropwise, and the mixture was stirred with warming to room temperature for 20 hours. The solid in the reaction solution was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (hexane:ethyl acetate=4:1) to afford the title compound (1.15 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409952B2
Source datasetuspto-grants-2016_08
ORD IDord-95b7bb491c5e4265ab91799331297610
Source noteuspto-grants-2016_08