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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489743생성일: 2026년 10월 25일

Triethylamine → (2S)-(4E)-5-(3-Pyridyl)-4-penten-2-ol

https://huagongshe.com/reaction/489743

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-BromopyridineHCID 12286—
반응물Tri-o-tolylphosphineHCID 80271—
반응물(S)-(+)-4-Penten-2-olHCID 6994332—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물(2S)-(4E)-5-(3-Pyridyl)-4-penten-2-olHCID 2065573763.3%

반응 조건

온도135 °C

반응 단계

A mixture of 3-bromopyridine (11.22 g, 70.58 mmol), (2S)-4-penten-2-ol (5.00 g, 58.05 mmol), palladium(II) acetate (527 mg, 2.35 mmol), tri-o-tolylphosphine (1.79 g, 5.88 mmol), triethylamine (30 mL, 216 mmol) and acetonitrile (30 mL) were heated in a sealed glass tube at 130-140° C. for 8 h. The reaction mixture was cooled to ambient temperature. The solvent was removed under reduced pressure on a rotary evaporator. Water (20 mL) was added and the mixture was extracted with chloroform (4×50 mL). The combined chloroform extracts were dried (K2CO3), filtered, and concentrated by rotary evaporation, producing a pale-yellow oil (6.00 g). The crude product was purified by column chromatography over silica gel, eluting with chloroform-acetone (95:5, v/v). Selected fractions were combined and concentrated by rotary evaporation, affording 3.95 g (41.7%) of a pale-yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06979695B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-9805064f5851449e8514ab9b5ccf5dfe
출처 메모uspto-grants-2005_12