돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127791생성일: 2026년 10월 25일

2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile → (1R,5S)-2,2,2-trichloroethyl-5-[[[(t-butyloxy)carbonyl]amino]oxy]-2-cyclopentene-1-carbamate

https://huagongshe.com/reaction/127791

반응식

참여 물질

역할이름HCID투입량
반응물2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
반응물(1R,5S)-2,2,2-trichloroethyl-5-(aminooxy)-2-cyclopentene-1-carbamateHCID 12943968—
용매TetrahydrofuranHCID 8028—
생성물(1R,5S)-2,2,2-trichloroethyl-5-[[[(t-butyloxy)carbonyl]amino]oxy]-2-cyclopentene-1-carbamateHCID 12943984—

반응 단계

An 7.8 g. quantity of crude (1R,5S)-2,2,2-trichloroethyl-5-(aminooxy)-2-cyclopentene-1-carbamate is dissolved in 25 ml. of tetrahydrofuran and 6.15 g (25 mm) of 2-(tertbutoxycarbonyloxyimino)-2-phenylacetonitrile and the mixture stirred for 22 hours at room temperature, 20 hours at 50° C., 72 hours at room temperature and then evaporated in vacuo. The residue is chromatographed over 900 g. of silica gel eluted with (15-85) ethylacetate-toluene. Three hundred ml. fractions are collected. The product is found in fractions 10-12. Evaporation and recrystallization of the residue from Skellysolve B yields (1R,5S)-2,2,2-trichloroethyl-5-[[[(t-butyloxy)carbonyl]amino]oxy]-2-cyclopentene-1-carbamate m.p. 83°-84° C. as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04256898
출처 데이터셋uspto-grants-1981_03
ORD IDord-75ee6477c97849189c49e6414904e58d
출처 메모uspto-grants-1981_03