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HRID 455899作成日:2026年10月25日

Benzyl Alcohol → (1-Benzyloxycarbonylmethyl-cyclohexyl)-acetic acid

https://huagongshe.com/reaction/455899

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物PyridineHCID 1049—
反応物TolueneHCID 1140—
反応物1,1-Cyclohexanediacetic AnhydrideHCID 2734289—
生成物(1-Benzyloxycarbonylmethyl-cyclohexyl)-acetic acidHCID 1403666990.1%

反応条件

温度80 °C

反応手順

A mixture of 1,1-cyclohexanediacetic anhydride (5.0 g, 27 mmol), pyridine (2.2 mL, 27 mmol), and benzyl alcohol (2.8 mL, 27 mmol) and toluene (5.0 mL, 47 mmol) was stirred at 80° C. overnight. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate and 1 N HCl. The organic layer was washed three times with 1 N HCl and brine. The organic extract was dried over sodium sulfate, filtered, and concentrated to dryness to yield the title compound (7.06 g, 89% yield) as a clear oil. 1H NMR (DMSO-d6, 400 mHz) δ (ppm): 11.96 (s, 1H), 7.32 (m, 5H), 5.03 (s, 2H), 2.52 (s, 2H), 2.34 (s, 2H), 1.40 (m, 10H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08497287B2
出典データセットuspto-grants-2013_07
ORD IDord-8287b0aa26ad4d9bbe918e5f7b621dd1
出典メモuspto-grants-2013_07