HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589962Generated: October 30, 2026
tert-Butanol → tert-butyl N-(chlorosulfonyl)carbamate
https://huagongshe.com/reaction/589962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | tert-butyl N-(chlorosulfonyl)carbamate | HCID 15677406 | — |
Reaction Steps
N-(oxomethylene)sulfamoyl chloride (13.4 mmol) was dissolved in dry benzene (5 mL) and dropwise added t-BuOH (13.4 mmol) while the temperature was kept below 25° C. The reaction mixture was stirred at 25° C. for 2 h, added hexane (5 mL) and cooled to 0° C. Precipitate was collected by filtration, washed with hexane affording tert-butyl N-chlorosulfonylcarbamate as white crystals. 4-(4,7-diaza-spiro[2.5]oct-7-yl)-7H-pyrrolo[2,3-d]pyrimidine (4.6 mmol) (intermediate 21) was suspended in dry DCM (25 mL) and added triethylamine (6.9 mmol). To this suspension was slowly added tert-butyl N-chlorosulfonylcarbamate (4.6 mmol) at rt. After 15 min all starting material has been consumed. The obtained reaction mixture was concentrated in vacuo on celite. The product was purified by flash chromatography on silica using EtOAc:MeOH in heptane as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233964B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-adbc00b6728a4e0c93d71fadf89f3f15 |
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| Source note | uspto-grants-2016_01 |
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