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HRID 45272作成日:2026年10月24日

Urea → Benzenepropanal

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

反応式

関与物質

役割名称HCID仕込み量
反応物UreaHCID 1176—
反応物2-Bromo-3-phenylpropanalHCID 11390228—
反応物5-Benzyloxazol-2-amineHCID 60027526—
溶媒EthanolHCID 702—
生成物BenzenepropanalHCID 7707—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541453B2
出典データセットuspto-grants-2013_09
ORD IDord-a7cd14ff2615466eafaf4d5b09a4529c
出典メモuspto-grants-2013_09