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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333322생성일: 2026년 10월 24일

Benzyl Bromide → HCID 68753687, 화합물

https://huagongshe.com/ko/reaction/333322

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물2(4-Biphenyl)propionic acidHCID 3082434—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 68753687HCID 6875368788.1%

반응 단계

To a suspension of 3-(biphenyl-4-yl)propanoic acid (5 g, 22.10 mmol) and K2CO3 (6.11 g, 44.2 mmol) in DMF (22 ml), BnBr (3.94 ml, 33.1 mmol) was added. After stirred for 15 hours, additional BnBr (3.94 ml, 33.1 mmol) was added. After stirred for further 22 hours, the reaction was diluted with H2O, extracted with EtOAc, washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The obtained residue was diluted with EtOAc (150 ml), and NH-silica gel was added to the suspension. The EtOAc was evaporated, and the resulted slurry was allowed to stir for 1 hour. The slurry was eluted with 10% EtOAc/heptane (150 ml) to give benzyl 3-(biphenyl-4-yl)propanoate (6.16 g); Retention time=1.71 minutes (condition A); 1H NMR (400 MHz, CDCl3) δ ppm 2.72 (t, J=7.8 Hz, 2H) 3.01 (t, J=7.8 Hz, 2H) 5.12 (s, 2H) 7.21-7.47 (m, 14H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877815B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-b78513581fb14ee78dd3ce13c4628a39
출처 메모uspto-grants-2014_11