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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1252225생성일: 2026년 10월 27일

Triethylamine → 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol

https://huagongshe.com/reaction/1252225

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acidHCID 13334384—
용매TetrahydrofuranHCID 8028—
생성물4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanolHCID 20140800—

반응 단계

To a mixture of 4-methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid (14.0 g) and triethylamine (5.25 g) in tetrahydrofuran (280 ml), ethyl chloroformate (5.64 g) was added with ice-cooling and then stirred for 30 minutes. The resulting triethylamine hydrochloride was removed by filtration. To filtrate was added sodium borohydride (5 g) in water (90 mg) with ice-cooling, and the mixture was stirred for 1.5 hours. The reaction mixture was concentrated to a volume of 120 ml in vacuo and extracted with dichloromethane. The dichloromethane layer was washed with diluted hydrochloric acid and then water, dried over anhydrous sodium sulfate and evaporated in vacuo to give an oily residue which was then purified by silica gel chromatography to give 4-methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04742052
출처 데이터셋uspto-grants-1988_05
ORD IDord-aeb5bb4dba7b42c5bfeaebee6c17486c
출처 메모uspto-grants-1988_05