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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45272생성일: 2026년 10월 24일

Urea → Benzenepropanal

https://huagongshe.com/ko/reaction/45272

반응식

참여 물질

역할이름HCID투입량
반응물UreaHCID 1176—
반응물2-Bromo-3-phenylpropanalHCID 11390228—
반응물5-Benzyloxazol-2-amineHCID 60027526—
용매EthanolHCID 702—
생성물BenzenepropanalHCID 7707—

반응 단계

5-Benzyl-oxazol-2-ylamine A mixture of 2-bromo-3-phenylpropionaldehyde (14.2 g, crude from above) and urea (7.2 g, 0.12 mol) were heated at reflux for 15 hours in 200 mL of ethanol. The solvent was evaporated to dryness and the residue was diluted with dichloromethane (250 mL) and then washed with sodium hydroxide (10% aqueous solution, 100 mL) and water (50 mL). The organic layer was washed three times with hydrochloric acid (5% aqueous solution, 250 mL). The combined aqueous layers were brought to pH 9 to 10 with a 10% aqueous solution of sodium hydroxide and then extracted three times with dichloromethane (300 mL). The organic layer was dried over sodium sulfate, evaporated to dryness, and purified by silica gel column chromatography to give a pale yellow solid (1.6 g, 9.2 mmol, 9.2% from 3-phenyl-propionaldehyde). ESI-MS m/z calc. 174.1. found 175.1 (M+1)+; 1H NMR (CDCl3) δ 7.32-7.22 (m, 5H), 6.39 (s, 1H), 4.72 (bs, 2H), 3.84 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541453B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a7cd14ff2615466eafaf4d5b09a4529c
출처 메모uspto-grants-2013_09