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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantHexaneHCID 8058—
ReactantChlorosulfonyl isocyanateHCID 70918—
SolventBenzeneHCID 241—
Producttert-butyl N-(chlorosulfonyl)carbamateHCID 15677406—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233964B2
Source datasetuspto-grants-2016_01
ORD IDord-adbc00b6728a4e0c93d71fadf89f3f15
Source noteuspto-grants-2016_01