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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256683생성일: 2026년 10월 26일

Hydrochloric Acid → Benzyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylate

https://huagongshe.com/reaction/256683

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylateHCID 15640822—
촉매Titanium(IV)ethoxideHCID 2724286—
용매Benzyl AlcoholHCID 244—
용매WaterHCID 962—
생성물Benzyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylateHCID 18957067143.5%

반응 단계

A solution of 1.62 9 of tetraethyl orthotitanate in 71 ml of benzyl alcohol was treated with 4.52 g of methyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylate and stirred at 115°-120° under argon for 3 hours. The reaction mixture was then cooled, stirred with 71 ml of 1N hydrochloric acid for 1 hour, diluted with 350 ml of water and extracted several times with methylene chloride. The organic phases were washed with saturated sodium hydrogen carbonate solution, dried over sodium sulphate, filtered and evaporated. The residue was stirred in 710ml of diethyl ether for 1 hour, suction filtered and the material obtained was dried in a vacuum. There was obtained 4.02g of benzyl 4,6-dihydro-4-oxo-3-phenylpyrido[2,1-a]isoindole-1-carboxylate as yellowish crystals with a m.p. of 229°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258387
출처 데이터셋uspto-grants-1993_11
ORD IDord-21cb10d88c6e42f7b4b0e618b702c92c
출처 메모uspto-grants-1993_11