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HRID 133450作成日:2026年10月26日

Cyclobutylcarbinol → Methyl 3-(4-chlorophenyl)-2-cyclobutylmethoxypropanoate

https://huagongshe.com/reaction/133450

反応式

関与物質

役割名称HCID仕込み量
反応物CyclobutylcarbinolHCID 78130—
反応物Methyl 2-diazo-3-(4-chlorophenyl)propanoateHCID 73879458—
溶媒BenzeneHCID 241—
生成物Methyl 3-(4-chlorophenyl)-2-cyclobutylmethoxypropanoateHCID 22270441—

反応条件

温度90 °C

反応手順

To a solution of 500 mg (2.23 mmol) of methyl-2-diazo-3-(4-chlorophenyl)propanoate (obtained from Step A) and 1.05 mL (5 eq; 11.1 mmol) of cyclobutanemethanol in 5 mL benzene in a pressure tube was added 10 mg (1 mole %) of Rh2(OAc)4 catalyst. The tube was sealed and heated to 90° C. for 1.5 h. The solvents were evaporated under reduced pressure and the crude material was taken up in CH2Cl2 and purified by flash chromatography via gradient elution using mixtures of hexane and EtOAc (100:1 to 50:1). This provided the title compound as a clear oil. TLC Rf=0.53 (4:1 hexanes:EtOAc). 500 MHz 1H NMR (CDCl3): δ 1.68 (m, 2H); 1.85 (m, 1H); 1.88 (m, 1H); 2.01 (m, 2H); 2.53 (sep, 1H); 2.98 (m, 2H); 3.24 (dd, 1H); 3.58 (dd, 1H); 3.76 (s, 3H); 3.98 (dd, 1H); 7.20 (d, 2H); 7.28 (d, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390835B2
出典データセットuspto-grants-2008_06
ORD IDord-3e7bf8543f6a4dd487f5a453cadb89a9
出典メモuspto-grants-2008_06