참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphate | HCID 1061 | — |
| 반응물 | 6-Nitro-2-toluonitrile | HCID 74669 | — |
| 반응물 | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Formyl-6-nitrobenzonitrile | HCID 86657474 | 19% |
반응 단계
1,1-Dimethoxy-N,N-dimethylmethanamine (13.56 mL, 102 mmol) was added to a solution of 2-methyl-6-nitrobenzonitrile (15.0 g, 92.5 mmol) in anhydrous DMF (60 mL) under nitrogen and was heated at 130° C. for 15 h. Ice water (300 mL) was added, and the resultant dark precipitate was collected by filtration and dried under vacuum. Phosphate buffer (pH 7, 350 mL) and then NaIO4 (40 g, 187 mmol) were added to a solution of the dark precipitate in THF (350 mL) and stirred at rt for 3 h. The mixture was extracted with EtOAc, the combined extract was washed with brine and dried with MgSO4. The filtrate was concentrated and the residue was purified by chromatography on silica using the solven gradient hexanes→EtOAc, to give 3.07 g (19%) of the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 8.15 (t, J=8.4 Hz, 1H), 8.41 (dd, J=1.2, 7.6 Hz, 1H), 8.62 (dd, J=1.2, 8.4 Hz, 1H), 10.25 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09181276B2 |
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| 출처 데이터셋 | uspto-grants-2015_11 |
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| ORD ID | ord-0ae6a3f30d2c468ca4577605f5f0987c |
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| 출처 메모 | uspto-grants-2015_11 |
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