戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 46889作成日:2026年10月25日

Potassium Iodide → 1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/46889

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Sodium CarbonateHCID 10340—
反応物4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
反応物1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 1810419—
溶媒WaterHCID 962—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-oneHCID 2038554326%

反応手順

A mixture of 2.3 parts of 1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one, 2.12 parts of 4-(4-chlorophenyl)-4-piperidinol, 3.2 parts of sodium carbonate, 0.1 parts of potassium iodide and 80 parts of 4-methyl-2-pentanone is stirred and refluxed for 36 hours. After cooling to room temperature, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from methylbenzene, yielding 1 part (26%) of 1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]-propyl}-1,3-dihydro-2H-benzimidazol-2-one; mp. 134.2° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04175129
出典データセットuspto-grants-1979_11
ORD IDord-74daae29ed5348479646a0fb34543927
出典メモuspto-grants-1979_11