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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 436432생성일: 2026년 10월 26일

Acetaldehyde → 1-(2-Ethylidenehydrazino)-3,4-dihydroisoquinoline

https://huagongshe.com/reaction/436432

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물EthanolHCID 702—
반응물Sulfuric AcidHCID 1118—
반응물1-Hydrazinyl-3,4-dihydroisoquinolineHCID 12349041—
용매Diethyl EtherHCID 3283—
생성물1-(2-Ethylidenehydrazino)-3,4-dihydroisoquinolineHCID 57269150—

반응 단계

A mixture of 1-ethoxy-3,4-dihydroisoquinoline (1.0 g.), hydrazine monohydrochloride (0.4 g.) and absolute ethanol (15 ml.) was heated under reflux (for 40 min.). The solution was cooled, filtered and concentrated and the residue was recrystallized from ethanol-ether, affording 1-hydrazino-3,4-dihydroisoquinoline hydrochloride (0.9 g., m.p. 205°-207° C.). C. A mixture of 1-hydrazino-3,4-dihydroisoquinoline (8.0 g.), acetaldehyde (20 ml.) and ethanol (20 ml.) was allowed to stand at room temperature (for 45 min). Ethanolic sulfuric acid was added until the solution was distinctly acidic. Ether was added. The resulting oil crystallized and the crystals were recrystallized from ethanol-ether, affording 1-(2-ethylidenehydrazino)-3,4-dihydroisoquinoline (I: X=CH3, X'=Y=Y'=Z=Z'=H) sulfate in two crops (8.3 g., m.p. 152°-154° C.; 0.5 g., m.p. 152°-155° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04009170
출처 데이터셋uspto-grants-1977_02
ORD IDord-094a02f11dc94b20987158205f53cf8c
출처 메모uspto-grants-1977_02