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HRID 7406作成日:2026年10月24日

Hexane → 1-Benzyl-4-(1-phenethyl-1H-imidazol-2-YL)piperidin-4-OL

https://huagongshe.com/ja/reaction/7406

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物1-Benzyl-4-piperidoneHCID 19220—
反応物1-(1-Phenylethyl)-1h-imidazoleHCID 9815351—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl-4-(1-phenethyl-1H-imidazol-2-YL)piperidin-4-OLHCID 1132590475%

反応条件

温度-70 °C

反応手順

A mixture of DIPA (1.4 mol) in THF (3000 ml) was stirred at −70° C. under N2 flow. Butyllithium 2.5 M/hexane (1.3 mol) was added portionwise at a temperature below −40° C. The mixture was stirred at −70° C. for 15 min. 1-phenylethyl-1H-imidazole (1 mol) dissolved in THF was added dropwise at a temperature below −55° C. The mixture was stirred at −70° C. for 1 hour. 1-(phenylmethyl)-4-piperidinone (1.2 mol) dissolved in THF was added dropwise at a temperature below −55° C. The mixture was stirred at −70° C. for 1 hour, then brought to room temperature, stirred at room temperature overnight and decomposed with H2O. The organic solvent was evaporated. The aqueous concentrate was extracted with CH2Cl2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue was crystallized from DIPE (1100 ml). The precipitate was filtered off, washed with DIPE and dried, yielding 271 g of 4-[1-(2-phenylethyl)-1H-imidazol-2-yl]-1-(phenylmethyl)-4-piperidinol (75%) (interm. 1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087595B2
出典データセットuspto-grants-2006_08
ORD IDord-b62c82ce4a9f497c902d1d7f12e1a2c2
出典メモuspto-grants-2006_08