참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-Hydroxy-3-phenylpropanoic acid | HCID 92959 | — |
| 반응물 | 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride | HCID 2734059 | — |
| 반응물 | (2-Nitrophenyl)methanamine hydrochloride | HCID 12235442 | — |
| 반응물 | Hydrate;hydrochloride | HCID 21885828 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amide | HCID 67461894 | 92.1% |
반응 단계
2-Nitrobenzyl amine hydrochloride (2.27 g, 12.0 mmol), 3-hydroxy-3-phenyl propionic acid (2.00 g, 12.0 mmol), triethylamine (1.34 g, 13.3 mmol) were added to tetrahydrofuran (50 ml) and the reaction mixture was ice cooled. Under ice cooled condition, 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (3.33 g, 12.0 mmol) was added thereto and stirred at room temperature for five hours. The reaction mixture was poured into dilute hydrochloric acid water and extracted with ethyl acetate. The organic layer was washed with a saturated brine and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained crude crystal was washed with a mixture of hexane-ether (2:1) to obtain 3-hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amide (3.32 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08048825B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-fc313c2da70d4e3490790ff94c8806ae |
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| 출처 메모 | uspto-grants-2011_11 |
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