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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29758생성일: 2026년 10월 23일

Triethylamine → Tert-butyl trans-4-(N-methoxy-N-methylcarbamoyl)cyclohexylcarbamate

https://huagongshe.com/ko/reaction/29758

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N,O-DimethylhydroxylamineHCID 14232—
반응물4-(((Tert-butoxy)carbonyl)amino)cyclohexane-1-carboxylic acidHCID 2755996—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Tert-butyl trans-4-(N-methoxy-N-methylcarbamoyl)cyclohexylcarbamateHCID 2472092861%

반응 단계

A solution of 4-[N-(tert-butoxycarbonyl)amino]-cyclohexane carboxylic acid (11.95 g, 49.0 mmol), O,N-dimethylhydroxylamine (4.88 g, 50.0 mmol), DCC (9.60 g, 50 mmol) and triethylamine (5.06 g, 50.0 mmol) in DMF (150 mL) was stirred at room temperature overnight. Water (500 mL) was added and the mixture was extracted with CHCl3. The organic phase was washed with water, dried and concentrated under reduced pressure. Purification by flash chromatography (hexane/EtOAc 1:1) gave [4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester (8.50 g, 61%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423012B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-c7af7f81ca4e42c0a273fa448c39b0b8
출처 메모uspto-grants-2008_09