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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 534824생성일: 2026년 10월 25일

Bromobenzene → Methyl 5-oxo-1-phenylprolinate

https://huagongshe.com/reaction/534824

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참여 물질

역할이름HCID투입량
반응물BromobenzeneHCID 7961—
반응물Carbonate IonHCID 19660—
반응물Methyl 5-oxo-DL-prolinateHCID 500249—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물Methyl 5-oxo-1-phenylprolinateHCID 4226099849%

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온도120 °C

반응 단계

A mixture of 5-oxo-pyrrolidine-2-carboxylic acid methyl ester (5.00 g, 34.9 mmol), bromobenzene (5.48 g, 34.9 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.96 g, 1.05 mmol), Xantphos™ (1.21 g, 2.09 mmol), and cecium carbonate (15.9 g, 48.9 mmol) in toluene (100 mL) was stirred at 120° C. for 20 h under argon atmosphere. The reaction mixture was cooled to room temperature, and partitioned between ethyl acetate and 2 M HCl solution. The organic layer was washed with saturated NaHCO3 solution, and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate 70:30 to 0:100) to give a yellow solid. The solid was triturated with hexane-diisopropyl ether to give the title compound (3.74 g, 49%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853215B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-dd26cb1e18be4408962ef6b7a9724af2
출처 메모uspto-grants-2014_10