HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189128Generated: October 30, 2026
tert-Butanol → tert-Butyl (benzylsulfamoyl)carbamate
https://huagongshe.com/reaction/2189128
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl (benzylsulfamoyl)carbamate | HCID 17757567 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324232B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-e131a55eb6d34e648fbb69dfcdf94b29 |
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| Source note | uspto-grants-2012_12 |
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