戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 487565作成日:2026年10月24日

Diethyl Ether → 1-(Cyclopropylmethyl)-4-(2'-(4"-fluorophenyl)-2'-phenyl-2'-hydroxyethyl)piperidine

https://huagongshe.com/ja/reaction/487565

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Ammonium ChlorideHCID 25517—
反応物DUP-734 free baseHCID 121968—
反応物HCID 178418255HCID 178418255—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Cyclopropylmethyl)-4-(2'-(4"-fluorophenyl)-2'-phenyl-2'-hydroxyethyl)piperidineHCID 19092168—

反応手順

1-(Cyclopropylmethyl)-4-(2'-(4"-fluorophenyl)-2'-oxoethyl)piperidine (Example 429, 1.0 g, 3.6 mmol) was mixed with dry tetrahydrofuran (10 mL). A solution of phenyl magnesium bromide in ether (3.0 M, 3 mL, 9 mmol) was added with stirring. The reaction mixture was stirred for 24 h; poured onto a saturated NH4Cl solution and extracted with ethyl acetate three times. The combined organic layers were dried over magnesium sulfate and filtered. Solvent was removed in vacuo. Trituration with ether-hexanes (1:9) and filtration afforded the title compound, a solid, which was dried in vacuo (0.9 g). mp 115°-116° C.; Anal. : Calcd for C23H28FNO: C, 77.36, H, 7.90, N, 3.92, F, 5.32; Found: C, 77.47, 77.41, H, 8.00, 7.92, N, 3.42, 3.52, F, 5.09.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05296479
出典データセットuspto-grants-1994_03
ORD IDord-89a59fa5a18a4c06b9c5c5c76d362443
出典メモuspto-grants-1994_03