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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 635639생성일: 2026년 10월 23일

Triacetoxyperiodinane → 3(S)-(tert-butoxyformamido)-2-oxo-N-(1(S)-phenylpropyl)heptanamide

https://huagongshe.com/ko/reaction/635639

반응식

참여 물질

역할이름HCID투입량
반응물TriacetoxyperiodinaneHCID 159087—
반응물3(S)-(tert-butoxyformamido)-2(S)-hydroxy-N-(1(S)-phenylpropyl)heptanamideHCID 20639979—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물3(S)-(tert-butoxyformamido)-2-oxo-N-(1(S)-phenylpropyl)heptanamideHCID 2063997770.6%

반응 단계

0.383 g of 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one was added to a solution of 0.285 g of 3(S)-(tert-butoxyformamido)-2(S)-hydroxy-N-(1(S)-phenylpropyl)heptanamide in 20 ml of dichloromethane. The mixture was stirred at room temperature for 30 minutes and then a further 30 mg of 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one were added. The mixture was stirred at room temperature for 30 minutes and then diluted with ethyl acetate. The solution was extracted with a solution of 10 g of sodium thiosulphate in 40 ml of saturated sodium bicarbonate solution. The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with water, dried over magnesium sulphate and evaporated. The residue was purified by chromatography on silica gel using 20% ethyl acetate in hexane for the elution to give 200 mg of 3(S)-(tert-butoxyformamido)-2-oxo-N-(1(S)-phenylpropyl)heptanamide, MS: m/e 377.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06187905B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-1f96bf04c2014bce81f9c620da14c3a0
출처 메모uspto-grants-2001_02