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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 541225생성일: 2026년 10월 27일

Methyl 2-bromo-4-methylbenzoate → Methyl 2-ethyl-4-methylbenzoate

https://huagongshe.com/reaction/541225

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 2-bromo-4-methylbenzoateHCID 21779704—
반응물HCID 178461630HCID 178461630—
촉매Zinc bromideHCID 10421208—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-ethyl-4-methylbenzoateHCID 6828877472%

반응 단계

To a stirred mixture of ZnBr2 (13 g, 57.72 mmol, 2.00 equiv) in THF (230 mL) under nitrogen at 0° C. was added dropwise EtMgBr (19.5 mL, 3 M in THF). After 30 minutes at 0° C., the temperature was lowered to −78° C. and Pd(dppf)Cl2 (2 g, 2.73 mmol, 0.09 equiv) was added followed by dropwise addition of a solution of methyl 2-bromo-4-methylbenzoate (6.6 g, 28.81 mmol, 1.00 equiv) in tetrahydrofuran (200 mL). The resulting mixture was allowed to slowly reach ambient temperature and stirred under nitrogen overnight. The reaction mixture was quenched by the careful addition of 20 mL NH4Cl (aq., sat.) and extracted with 3×100 mL of ethyl acetate. The combined organic layers were washed with 1×200 mL of brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified using silica gel column chromatography with ethyl acetate/petroleum ether (1:30) as eluent to yield 3.7 g (72%) of the title compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871790B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-b72143ae51a84c86b3769a1f451c8840
출처 메모uspto-grants-2014_10