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HRID 541225作成日:2026年10月27日

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

https://huagongshe.com/reaction/541225

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2-bromo-4-methylbenzoateHCID 21779704—
反応物HCID 178461630HCID 178461630—
触媒Zinc bromideHCID 10421208—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-ethyl-4-methylbenzoateHCID 6828877472%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871790B2
出典データセットuspto-grants-2014_10
ORD IDord-b72143ae51a84c86b3769a1f451c8840
出典メモuspto-grants-2014_10