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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 888561생성일: 2026년 10월 25일

Benzaldehyde → 2-(3-Bromo-phenyl)-3-phenyl-propionitrile

https://huagongshe.com/reaction/888561

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Potassium HydroxideHCID 14797—
반응물(3-Bromophenyl)acetonitrileHCID 36023—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물2-(3-Bromo-phenyl)-3-phenyl-propionitrileHCID 5933198152%

반응 단계

A solution of 40% KOH (2.83 g in 5.0 ml of H2O) in ethanol (13 ml) was added to a solution of benzaldehyde (2.85 ml, 28.05 mmol) and 3-bromophenylacetonitrile (5 g, 25.50 mmol) in ethanol (9 ml). The reaction mixture was then stirred at room temperature for 2 hours and the precipitate was collected by suction filtration and washed with cold ethanol (6.68 g, 92%). The crude product (3.45 g, 12.14 mmol) was then dissolved in ethanol (35 ml) and heated to 65° C. Sodium borohydride (459 mg, 12.14 mmol) was added in portions and the reaction mixture was maintained at this temperature for a further 2 hours. Upon cooling, water (10 ml) was added and the solvent was removed under reduced pressure. The residue was partitioned between water (100 ml) and ethyl acetate (100 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated to afford the desired product (1.80 g, 52%), which was used without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247576B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-b8d973987e364674877ad088b10f09a1
출처 메모uspto-grants-2012_08