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HRID 351439作成日:2026年10月24日

Hydrochloric Acid → 1-(4-Benzyloxy-phenyl)-2-ethyl-4-hydroxymethyl-3-methyl-cyclohexanol

https://huagongshe.com/ja/reaction/351439

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1-(Benzyloxy)-4-iodobenzeneHCID 519671—
反応物2-Ethyl-3-methyl-4-trimethylsilanyloxymethyl-cyclohexanoneHCID 18436335—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-(4-Benzyloxy-phenyl)-2-ethyl-4-hydroxymethyl-3-methyl-cyclohexanolHCID 18436325—

反応条件

温度25 °C

反応手順

1-Benzyloxy4-iodo-benzene (5.70 g, 18.37 mmol) was dissolved in anhydrous THF (36 mL) at −10° C. Isopropyl magnesium chloride (1.0 M, 18.37 mL) was added and the mixture was stirred for 3 h. A solution of 2-ethyl-3-methyl-4-trimethylsilanyloxymethyl-cyclohexanone (12.0 g in 50 mL THF) was added slowly over 30 min by syringe pump. The reaction mixture was stirred for 30 min at 25° C. and then refluxed for 30 min. The reaction mixture was then cooled to 25° C., HCl (1.0 N, 80 mL) was added slowly, followed by addition of ethyl acetate (100 mL). The organic layer was washed with H2O (100 mL), dried over MgSO4 and purified on SiO2 (10˜15% ethyl acetate/hexane) to yield 1-(4-benzyloxy-phenyl)-2-ethyl-4-hydroxymethyl-3-methyl-cyclohexanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07183445B2
出典データセットuspto-grants-2007_02
ORD IDord-c3d8936c17564bbeb3e9057aa27ba592
出典メモuspto-grants-2007_02