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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1684692생성일: 2026년 10월 26일

1,2-Epoxybutane → 3-Phenyl-2(S)-phthalimidopropan-1-al

https://huagongshe.com/reaction/1684692

반응식

참여 물질

역할이름HCID투입량
반응물1,2-EpoxybutaneHCID 7834—
반응물Sodium PyrosulfiteHCID 656671—
반응물3-phenyl-2(S)-phthalimidopropionyl chlorideHCID 10567197—
촉매PalladiumHCID 23938—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3-Phenyl-2(S)-phthalimidopropan-1-alHCID 11065801—

반응 단계

The solution containing the 3-phenyl-2(S)-phthalimidopropionyl chloride is diluted with 500 ml of toluene and treated with 72.11 g of 1,2-butylene oxide. 23.5 g of palladium-on-charcoal (5%) and 100 ml of toluene are added to the solution. The suspension is hydrogenated for 17 hours while stirring and then filtered, and the residue is washed with 200 ml of toluene. The filtrate and washings are combined and treated while stirring with a solution of 0.5 mol of sodium pyrosulfite in water. The phases are separated after 4.5 hours. The aqueous phase is washed with toluene. The toluene phases are washed with water. The combined aqueous phases are treated with toluene and 3N sulphuric acid and stirred at 60°. Thereafter, the phases are separated and the aqueous phase is extracted with toluene. The toluene phases are washed with water, combined, dried and evaporated. 3-Phenyl-2(S)-phthalimido-propan-1-al is obtained as a white solid, melting point 115°-117°, [a]D20 -200° (1% in ethyl acetate).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05641886
출처 데이터셋uspto-grants-1997_06
ORD IDord-9458e356afa94165ab9bff536f200665
출처 메모uspto-grants-1997_06