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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9403생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/9403

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-(4-aminobutyl)carbamateHCID 4351—
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
용매Acetic AcidHCID 176—
생성물Tert-butyl[4-(methanesulfonylamino)butyl]carbamateHCID 5418089996.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091214B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6adf18b19dfd401ca036b2c8938a2b96
출처 메모uspto-grants-2006_08