참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2,2-Dimethoxy-1-methylethylamine | HCID 93658 | — |
| 반응물 | 4-(Benzyloxy)-2-chloro-1-nitrobenzene | HCID 819861 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 2-[5-(Benzyloxy)-2-nitroanilino]propionaldehyde dimethyl acetal | HCID 19083116 | — |
반응 단계
A mixture of benzyl 3-chloro-4-nitrophenyl ether (48.2 g, 0.183 mole), 2-aminopropionaldehyde dimethyl acetal (65.3 g, 0.55 mole), potassium carbonate (101 g, 0.73 mole) and toluene in dry dimethyl sulfoxide, under nitrogen, is stirred at 99°-105° C. for 20 hours, cooled to room temperature and filtered. The filter cake is washed with ether. The combined filtrates are mixed with ice water. The phases are separated and the aqueous phase is extracted with ether. The ether extracts are combined with the organic phase. The combined organic phase is washed with six portions of water, dried (Na2SO4) and concentrated in vacuo to give an oil residue which is crystallized in methanol to afford the title product as a yellow solid, 39.6 g (64.5%). A sample is recrystallized from methanol to afford a yellow solid, mp 57°-62° C., identified by elemental and NMR analyses.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05763615 |
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| 출처 데이터셋 | uspto-grants-1998_06 |
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| ORD ID | ord-18fc9b6dbc484a6e8834325bb1a74df5 |
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| 출처 메모 | uspto-grants-1998_06 |
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