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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133450생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/133450

반응식

참여 물질

역할이름HCID투입량
반응물CyclobutylcarbinolHCID 78130—
반응물Methyl 2-diazo-3-(4-chlorophenyl)propanoateHCID 73879458—
용매BenzeneHCID 241—
생성물Methyl 3-(4-chlorophenyl)-2-cyclobutylmethoxypropanoateHCID 22270441—

반응 조건

온도90 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390835B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-3e7bf8543f6a4dd487f5a453cadb89a9
출처 메모uspto-grants-2008_06