참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Oxide | HCID 6354 | — |
| 반응물 | Diethylamine | HCID 8021 | — |
| 반응물 | 2-((4-Nitrophenoxy)methyl)oxirane | HCID 21327 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-Diethylamino-3-(4-nitro-phenoxy)-propan-2-ol | HCID 15072487 | 89% |
반응 단계
A solution of 2-(4-nitro-phenoxymethyl)-oxirane (9.75 g, 50 mmol) in absolute EtOH (100 mL) was heated at 70° C. until 2-(4-nitro-phenoxymethyl)-oxirane is dissolved then the solution was allowed to cool to room temperature. Subsequently the room temperature solution was treated with diethylamine (5.2 mL, 1.0 equiv.) in one portion. The reaction mixture is stirred at room temperature for 15 min during which time starting material (oxirane) began to precipitate out of solution. The reaction mixture was heated to 50° C. and an additional amount of diethylamine (2.6 mL) was added to achieve complete dissolution of starting oxirane. The reaction mixture was heated for an additional 5 h at 55° C. at which point thin layer chromatography (9:1, chloroform: methanol) indicated complete consumption of the starting oxirane. The reaction mixture was cooled to room temperature and concentrated in vacuo. The oily light brown residue obtained after evaporation, was purified by flash silica gel chromatography, (CHCl3 to 1:9, MeOH:CHCl3 gradient eluant) to give the 1-diethylamino-3-(4-nitro-phenoxy)-propan-2-ol as a yellow oil (11.9 g, 89%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07692005B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-985ad3c7462549748d6aac79e615bd54 |
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| 출처 메모 | uspto-grants-2010_04 |
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