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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70519생성일: 2026년 10월 23일

Triphenylphosphine → (R)-5-{[(1-phenyl-1H-tetrazol-5-yl)sulfanyl]methyl}pyrrolidin-2-one

https://huagongshe.com/ko/reaction/70519

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(R)-(-)-5-(Hydroxymethyl)-2-pyrrolidinoneHCID 7128291—
반응물1-phenyltetrazole-5-thiolHCID 178527986—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물(R)-5-{[(1-phenyl-1H-tetrazol-5-yl)sulfanyl]methyl}pyrrolidin-2-oneHCID 6739903918.4%

반응 단계

1-Phenyl-1H-tetrazole-5-thiol (9.0 g) and triphenylphosphine (13.2 g) were added to a solution of (R)-(−)-5-(hydroxymethyl)-2-pyrrolidinone (4.5 g) in tetrahydrofuran (90 mL), followed by ice-cooling. A solution of 2.2 M diethyl azodicarboxylate in toluene (23 mL) was added dropwise thereto, and the mixture was stirred at room temperature overnight. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=4:1→1:1→0:1) to give (R)-5-{[(1-phenyl-1H-tetrazol-5-yl)sulfanyl]methyl}pyrrolidin-2-one (1.98 g) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822503B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6e99fe8f850f46e2b4753643d346aefa
출처 메모uspto-grants-2014_09