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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189128Generated: October 30, 2026

tert-Butanol → tert-Butyl (benzylsulfamoyl)carbamate

https://huagongshe.com/reaction/2189128

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantBenzylamineHCID 7504—
ReactantChlorosulfonyl isocyanateHCID 70918—
SolventDichloromethaneHCID 6344—
Producttert-Butyl (benzylsulfamoyl)carbamateHCID 17757567—

Reaction Conditions

Temperature0 °C

Reaction Steps

Chlorosulfonylisocyanate (14.14 g) was dissolved in DCM (50 mL) and cooled to 0° C. A solution of t-BuOH (9.6 mL) in DCM (50 mL) was added within 30 min. Stirring was continued for additional 30 min at rt. The solution thus obtained was then added at 0° C. within 1 h to a solution of benzylamine (10.7 g) and TEA (15.32 mL) in DCM (200 mL). Stirring is continued for 10 h at rt. The mixture was concentrated in vacuo, taken up in EA (500 mL) and washed with water (2×40 mL) and brine (30 mL), dried over MgSO4, filtered. The filtrate was concentrated in vacuo and the crude material was crystallized from EA and dried under HV to give N-benzyl-N′-tert-butoxycarbonyl sulfamide (13.68 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324232B2
Source datasetuspto-grants-2012_12
ORD IDord-e131a55eb6d34e648fbb69dfcdf94b29
Source noteuspto-grants-2012_12