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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | 1-Chlorobenzotriazole | HCID 88761 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | N-(tert-butoxycarbonyl)-2-aminoethanethiol | HCID 3017761 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl (2-(tert-butyldisulfanyl)ethyl)carbamate | HCID 89668308 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409952B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-95b7bb491c5e4265ab91799331297610 |
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| Source note | uspto-grants-2016_08 |
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