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HRID 5783作成日:2026年10月24日

2-Chloroethyl methyl ether → (2-methoxyethyl) 1-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-imidazole-5-carboxylate

https://huagongshe.com/ja/reaction/5783

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloroethyl methyl etherHCID 12316—
反応物Sodium hydrideHCID 24758—
反応物3-(1,2,3,4-Tetrahydro-naphthalen-1-yl)-3H-imidazole-4-carboxylic acidHCID 19794079—
溶媒DimethylformamideHCID 6228—
生成物(2-methoxyethyl) 1-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-imidazole-5-carboxylateHCID 5376576646.7%

反応手順

4.8 Parts of 1-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-imidazole-5-carboxylic acid are dissolved in 94 parts of warm N,N-dimethylformamide. 0.96 Parts of a sodium hydride dispersion 50% are added portionwise to the thus obtained reaction mixture. Upon complete addition, stirring is continued for 1 hour at room temperature. After the addition of 2.0 parts of 1-chloro-2-methoxyethane, the whole is stirred overnight at 90° C. The reaction mixture is evaporated and the residue is taken up in water. The product is extracted with trichloromethane. The extract is dried, filtered and evaporated, yielding 2.8 parts (46.7%) of (2-methoxyethyl) 1-(1,2,3,4-tetrahydro-1-naphthalenyl)-1H-imidazole-5-carboxylate; mp. 66.8° C. (compound 1.83).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246915
出典データセットuspto-grants-1993_09
ORD IDord-4af060a23de24f8e80acbb43ee1a8a58
出典メモuspto-grants-1993_09