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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818153Generated: October 26, 2026

tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl[4-(methanesulfonylamino)butyl]carbamate

https://huagongshe.com/reaction/1818153

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventAcetic AcidHCID 176—
ProductTert-butyl[4-(methanesulfonylamino)butyl]carbamateHCID 5418089996.7%

Reaction Steps

Under a nitrogen atmosphere, a solution of tert-butyl N-(4-aminobutyl)carbamate (13.8 g, 73.4 mmol) and triethylamine (15.3 mL, 110 mmol) was cooled to 0° C. Methanesulfonyl chloride (6.3 mL, 81 mmol) was added, and the reaction was allowed to warm to ambient temperature and stirred overnight. Aqueous acetic acid (200 mL of 10%) was added. The organic layer was then separated and washed with water (200 mL), saturated aqueous sodium bicarbonate (200 mL), water (200 mL), and brine; dried over sodium sulfate; filtered; and concentrated under reduced pressure to provide 18.9 g of tert-butyl [4-(methanesulfonylamino)butyl]carbamate as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598382B2
Source datasetuspto-grants-2009_10
ORD IDord-90e90b73f60a4fca8967d86921d4878b
Source noteuspto-grants-2009_10