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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3989생성일: 2026년 10월 23일

2,3-Dihydroxybutanedioic Acid → 2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde

https://huagongshe.com/ko/reaction/3989

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dihydroxybutanedioic AcidHCID 875—
반응물Sulfuric AcidHCID 1118—
반응물Potassium HydroxideHCID 14797—
반응물5-[Methyl(2-phenylethyl)amino]-2-phenyl-2-propan-2-ylpentanenitrileHCID 71225—
반응물DiisobutylaluminumhydrideHCID 21225700—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehydeHCID 88638019—

반응 단계

180 ml of a 1M solution of diisobutylaluminum hydride in hexane were added dropwise, at -5° C., to a solution of 33.4 g (0.1 mole) of 2-[3-[(phenylethyl)-methylamino]-propyl]-isopropylphenylacetonitrile in 400 ml of diethyl ether. The mixture was stirred for 1.5 hours, after which 500 ml of 10% strength sulfuric acid were added. 30 g of tartaric acid were introduced, the mixture was rendered alkaline with concentrated potassium hydroxide solution, and the ether phase was separated off and washed several times with sodium chloride solution. After the ether phase had been dried over sodium sulfate, the ether was distilled off, the remaining oily residue was dissolved in 300 ml of ethyl acetate, and hydrochloric acid in isopropanol was added. The mixture was left to stand overnight, after which the precipitated hydrochloride was filtered off under suction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723039
출처 데이터셋uspto-grants-1988_02
ORD IDord-9e27edb996dc4b2e8698c669aeab451a
출처 메모uspto-grants-1988_02