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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 858927생성일: 2026년 10월 25일

Triphenylphosphine → Triphenylphosphine

https://huagongshe.com/reaction/858927

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Triphenylphosphine OxideHCID 13097—
반응물3-Fluorobenzylic alcoholHCID 68008—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물HCID 785701HCID 785701—
용매TetrahydrofuranHCID 8028—
생성물TriphenylphosphineHCID 11776—
생성물Diisopropyl bicarbamateHCID 88220—
생성물(S)-1-[4-(3-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methyl esterHCID 68614551—

반응 단계

A solution of 110.6 mmol of 3-fluoro-benzylalcohol and 108.8 mmol of triphenylphosphine in 150 ml of tetrahydrofuran was added dropwise, within 50 min under a nitrogen atmosphere at 0° C., to a solution of 100.5 mmol of (S)-1-(4-hydroxy-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester and 100.5 mmol of diisopropyl azodicarboxylate in 200 ml of tetrahydrofuran. The mixture was left to warm to RT and stirring was continued for 18 hours. The mixture was evaporated under reduced pressure. The solid residue was triturated in 400 ml of ether to leave a white solid mainly consisting of the product and triphenylphosphinoxide. After filtration, the solid material was triturated in 100 ml of cold methanol to yield (S)-1-[4-(3-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methyl ester as a white solid [MS: m/e=344 (M+H)+] together with traces of triphenylphosphine and diisopropyl hydrazodicarboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07148362B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-052cf91d6ead4b40a5385415d5ed7399
출처 메모uspto-grants-2006_12