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HRID 351441作成日:2026年10月26日

Hydrogen Peroxide → 2-(4-Benzyloxy-phenyl)-3-ethyl-5-hydroxymethyl-4-methyl-cyclohexanol

https://huagongshe.com/reaction/351441

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Dimethyl SulfideHCID 1068—
反応物Sodium HydroxideHCID 14798—
反応物[4-(4-Benzyloxy-phenyl)-5-ethyl-6-methyl-cyclohex-3-enyl]-methanolHCID 18436344—
溶媒TetrahydrofuranHCID 8028—
溶媒Water ethylacetateHCID 22728543—
生成物2-(4-Benzyloxy-phenyl)-3-ethyl-5-hydroxymethyl-4-methyl-cyclohexanolHCID 18436333—

反応条件

温度0 °C

反応手順

To the solution of [4-(4-benzyloxy-phenyl)-5-ethyl-6-methyl-cyclohex-3-enyl]-methanol (3.1 g, 6.8 mmol) in THF (50 mL) was added BH3.S(CH3)2 solution (1.0 M in THF, 10.3 mL, 1.5 eq.) at 0° C. The reaction mixture was refluxed for 4 h and then cooled to 0° C. NaOH (20% aqueous, 30 mL) and H2O2 (50% in H2O, 21 mL) were added at 0° C. The reaction mixture was then stirred at 0˜25° C. for 4 h. The reaction mixture was then diluted with ethyl acetate/H2O (400 mL/200 mL). The organic layer was separated, dried over MgSO4 and purified on SiO2 (50˜100% ethyl acetate/hexane) to yield 2-(4-benzyloxy-phenyl)-3-ethyl-5-hydroxymethyl-4-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-73f1c5ea53c54f169e78a3de55763651
出典メモuspto-grants-2007_02