戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2113161作成日:2026年10月25日

Hydrochloric Acid → 1-(4-Benzyloxy-3-chlorophenyl)-2,2,2-trifluoroethanol

https://huagongshe.com/reaction/2113161

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物(Trifluoromethyl)trimethylsilaneHCID 552549—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物4-(Benzyloxy)-3-chlorobenzaldehydeHCID 2735495—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-(4-Benzyloxy-3-chlorophenyl)-2,2,2-trifluoroethanolHCID 69050976—

反応条件

温度25 °C

反応手順

To a solution of 4-benzyloxy-3-chlorobenzaldehyde (4.9 g, 20 mmol) and trimethyl(trifluoromethyl)silane (4.4 mL, 30 mmol) in THF (0.10 L) was added a solution tetrabutylammonium fluoride (1.0 M in THF, 2.0 mL). After the reaction was stirred at 25° C. for 3 h, it was acidified with 2 N HCl to pH 2, diluted with ethyl acetate and washed with brine. The organic phase was dried and concentrated and the residue was purified by chramotography on silica gel eluting with 8:2 hexane:ethyl acetate to give 1-(4-benzyloxy-3-chlorophenyl)-2,2,2-trifluoroethanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07524882B2
出典データセットuspto-grants-2009_04
ORD IDord-b99b7676da0141c19ba218f3fcf51726
出典メモuspto-grants-2009_04