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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4256생성일: 2026년 10월 24일

tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamate → (3RS,4S)-4-(tert-butoxycarbonyl)amino-6-methylhepten-3-ol

https://huagongshe.com/ko/reaction/4256

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamateHCID 104275—
반응물HCID 178418507HCID 178418507—
용매TetrahydrofuranHCID 8028—
생성물(3RS,4S)-4-(tert-butoxycarbonyl)amino-6-methylhepten-3-olHCID 1385604965%

반응 단계

To a stirred 0° C. solution of Boc-leucinal (3.00 g, 13.9 mmol) in dry tetrahydrofuran (THF) (70 ml) was added vinyl magnesium bromide (35 ml of a 1.0M solution in THF). After 5 hours, the mixture was quenched with 1.0M NH4Cl (50 ml). Most of the THF was evaporated in vacuo and the residue was extracted with ether several times. The combined extracts were washed (brine), dried (Na2SO4), filtered, and evaporated to give the desired product as a 3:2 mixture of hydroxy diastereomers in 65% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04725583
출처 데이터셋uspto-grants-1988_02
ORD IDord-5281eca835b24f4999f7ce801feb6dce
출처 메모uspto-grants-1988_02