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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1901338생성일: 2026년 10월 26일

Triphenylphosphine → Ethyl 2-[4-[((2S)-1-tert-butoxycarbonyl-2-pyrrolidinyl)methoxy]phenyl]-3-(5-cyano-2-benzofuranyl)propionate

https://huagongshe.com/reaction/1901338

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(S)-(-)-N-Boc-prolinolHCID 643448—
반응물Ethyl 3-(5-cyano-2-benzofuranyl)-2-(4-hydroxyphenyl)propionateHCID 21844506—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-[4-[((2S)-1-tert-butoxycarbonyl-2-pyrrolidinyl)methoxy]phenyl]-3-(5-cyano-2-benzofuranyl)propionateHCID 5728660251.1%

반응 단계

1.04 g of diethyl azodicarboxylate was added to 300 ml of a tetrahydrofuran solution containing 1 g of ethyl 3-(5-cyano-2-benzofuranyl)-2-(4-hydroxyphenyl)propionate, 1.2 g of (2S)-1-tert-butoxycarbonyl-2-pyrrolidinemethanol and 1.56 g of triphenylphosphine, and the thus prepared mixture was stirred at room temperature for 18 hours. To the resulting reaction solution were added 0.6 g of (2S)-1-tert-butoxycarbonyl-2-pyrrolidinemethanol, 0.78 g of triphenylphosphine and 0.52 g of diethyl azodicarboxylate, followed by additional stirring at room temperature for 18 hours. Thereafter, the reaction solution thus obtained was concentrated to dryness, and the resulting residue was purified by subjecting it to silica gel column chromatography using a toluene/ethyl acetate mixture as an eluant. In this way, 790 mg of the title compound was obtained in the form of colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05576343
출처 데이터셋uspto-grants-1996_11
ORD IDord-9f81d53f06e04d7abb8b50afe1573dad
출처 메모uspto-grants-1996_11