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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1799205생성일: 2026년 10월 26일

Potassium Phosphate, Tribasic → 4-[5-((3R)-5-oxopyrrolidin-3-yl)-2-chlorophenyl]benzoic acid

https://huagongshe.com/reaction/1799205

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물4-Methoxycarbonylphenylboronic acidHCID 2734369—
반응물(4R)-4-(3-bromo-4-chlorophenyl)pyrrolidin-2-oneHCID 66724952—
촉매Tetrabutylammonium BromideHCID 74236—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-[5-((3R)-5-oxopyrrolidin-3-yl)-2-chlorophenyl]benzoic acidHCID 66725141—

반응 조건

온도90 °C

반응 단계

(4R)-4-(3-Bromo-4-chlorophenyl)pyrrolidin-2-one (0.5 g, 0.55 mmol) and 4-methoxycarbonylphenyl boronic acid (0.144 g, 0.55 mmol) were mixed in DMF (2 mL). The mixture was degassed by alternately applying a vacuum and flushing with nitrogen gas. Palladium acetate (0.025 g, 0.11 mmol) and tetrabutylammonium bromide (0.053 g, 0.165 mmol) were added followed by potassium phosphate (0.35 g, 1.65 mmol). The mixture was stirred overnight at 90° C. The reaction mixture was cooled to room temperature, diluted with ethyl acetate (50 mL), washed with 10% aqueous HCl solution then brine, and concentrated in vacuo to provide 4-[5-((3R)-5-oxopyrrolidin-3-yl)-2-chlorophenyl]benzoic acid. 4-[5-((3R)-5-Oxopyrrolidin-3-yl)-2-chlorophenyl]benzoic acid was then treated with HCl as described for the preparation of (3R)-4-amino-3-(3-bromo-4-chlorophenyl)butanoic acid hydrochloride to provide the title compound (24). MS (ESI) m/z 334.07 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08344028B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-836e300eda1443bc8729141dc580c4a6
출처 메모uspto-grants-2013_01