Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Salicylaldehyde → 3-Hydroxy-3-{1-[(2-hydroxybenzylidene)amino]ethyl}pyrrolidine-1-carboxylic acid benzyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Salicylaldehyde | HCID 6998 | — |
| 반응물 | 3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester | HCID 69068640 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 3-Hydroxy-3-{1-[(2-hydroxybenzylidene)amino]ethyl}pyrrolidine-1-carboxylic acid benzyl ester | HCID 136330327 | 35% |
반응 단계
A solution of 3-(1-aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester (Example A10, 0.34 g, 0.93 mmol) and salicylaldehyde (0.147 g, 1.2 mmol) in dry ethanol (5 mL) is refluxed for 3 hours. After evaporation of the solvent, the residue is purified by column chromatography (30:70:0.01 ethyl acetate/hexanes/ammonium hydroxide) to afford the title compound (0.12 g). 1H NMR (200 MHz, CDCl3): δ 8.39 (s, 1H), 7.41–7.25 (m, 7H), 6.97–6.85 (m, 2H), 5.09 (s, 2H), 3.65–3.34 (m, 5H), 2.01–1.87 (m, 2H), 1.37–1.32 (m, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07094780B1 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-59aeace69c524501960f8f1eb266305a |
| 출처 메모 | uspto-grants-2006_08 |