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HRID 344060作成日:2026年10月26日

Pyridine → 2-[(5-Ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methoxycarbonyl]-1,1-diphenylhydrazine

https://huagongshe.com/reaction/344060

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物PhosgeneHCID 6371—
反応物Hydrazine, 1,1-diphenyl-, hydrochloride (1:1)HCID 10738—
反応物(5-Ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methanolHCID 53647005—
溶媒DichloromethaneHCID 6344—
生成物2-[(5-Ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methoxycarbonyl]-1,1-diphenylhydrazineHCID 70187314—

反応手順

To a methylene chloride solution (1 ml) of phosgene dimer (0.027 ml) was added a methylene chloride solution (2 ml) of (5-ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methanol (0.12 g) and pyridine (0.1 ml) at -5° C., and the solution was stirred at room temperature for two hours. To the reaction mixture was added a solution of 1,1-diphenylhydrazine hydrochloride (0.10 g) and pyridine (0.05 ml) in methylene chloride (2 ml). The solution was stirred at room temperature for 3 hours, washed with 5% hydrochloric acid, water, and brine, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed (n-hexane-ethyl acetate) over silica gel to afford 2-[(5-ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methoxycarbonyl]-1,1-diphenyihydrazine (0.13 g) as colorless solids.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05863918
出典データセットuspto-grants-1999_01
ORD IDord-5434fa9b16764b019f4f78cd116bcaef
出典メモuspto-grants-1999_01