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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 977244생성일: 2026년 10월 27일

Dichloromethane → 2-Acetoxy-4-[4-[3-(5-methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]butyronitrile

https://huagongshe.com/reaction/977244

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium CyanideHCID 8929—
반응물3-[4-[3-(5-Methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]propionaldehydeHCID 19965627—
촉매Benzyltributylammonium chlorideHCID 159952—
용매WaterHCID 962—
생성물2-Acetoxy-4-[4-[3-(5-methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]butyronitrileHCID 1996564399.3%

반응 단계

A mixture of 3-[4-[3-(5-methyl-2-phenyl-4-oxazolyl)propionyl]phenyl]propionaldehyde (1.47 g), sodium cyanide (0.25 g), acetic anhydride (0.52 g), benzyltributylammonium chloride [(C4H9)3 (C6H5CH2)N+Cl- ](0.66 g) and dichloromethane (30 ml)- water (10 ml) was stirred at room temperature for 18 hours. The organic layer was separated, washed with water, dried (MgSO4) and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-hexane (1:2), 2-acetoxy-4-[4-[3-(5-methyl- 2-phenyl-4-oxazolyl)propionyl]phenyl]butyronitrile (1.75 g, quantitative) was obtained as an oily substance. NMR (δ ppm in CDCl3): 2.13 (3H, s), 2.15-2.3 (2H, m), 2.38 (3H, s), 2.8-3.0 (4H, m), 3.39 (2H, t, J=7 Hz), 5.29 (1H, t, J=6.5 Hz), 7.28 (2H, d, J=8 Hz), 7.35-7.5 (3H, m), 7.9-8.05 (4H, m)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05614544
출처 데이터셋uspto-grants-1997_03
ORD IDord-c8edab1bf1d841d89251980e8e93f5cf
출처 메모uspto-grants-1997_03