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HRID 436432作成日:2026年10月26日

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

https://huagongshe.com/reaction/436432

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物EthanolHCID 702—
反応物Sulfuric AcidHCID 1118—
反応物1-Hydrazinyl-3,4-dihydroisoquinolineHCID 12349041—
溶媒Diethyl EtherHCID 3283—
生成物1-(2-Ethylidenehydrazino)-3,4-dihydroisoquinolineHCID 57269150—

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04009170
出典データセットuspto-grants-1977_02
ORD IDord-094a02f11dc94b20987158205f53cf8c
出典メモuspto-grants-1977_02