Identification | Back Directory | [Name]
2-METHOXY-5-NITROBENZALDEHYDE | [CAS]
25016-02-8 | [Synonyms]
AKOS B028867 5-Nitro-o-anisaldehyde 5-Nitro-o-anisaldehyde 2-METHOXY-5-NITROBENZALDEHYDE 2-methoxy-5-nitro-benzaldehyd Benzaldehyde, 2-methoxy-5-nitro- 4-(4-morpholinyl)-6-[[4-(phenylmethyl)-1-piperazinyl]methyl]-1,3,5-triazin-2-amine | [Molecular Formula]
C8H7NO4 | [MDL Number]
MFCD02093683 | [MOL File]
25016-02-8.mol | [Molecular Weight]
181.15 |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 2-methoxy-5-nitrobenzaldehyde from 5-nitrosalicylaldehyde and iodomethane: Sodium hydride (NaH, 246 mg) and iodomethane (2.56 g) were added to a solution of 5-nitrosalicylaldehyde (1.00 g, 6.0 mmol) in N,N-dimethylformamide (DMF, 20 ml). The reaction mixture was stirred at 0°C for 8.5 hours. After completion of the reaction, the reaction mixture was extracted with ether and the organic phase was washed sequentially with aqueous sodium bicarbonate, saturated brine and 5% hydrochloric acid/saturated brine. The organic phase was dried with anhydrous magnesium sulfate and concentrated under reduced pressure to give 2-methoxy-5-nitrobenzaldehyde (0.95 g, 87.8% yield) as yellow needle-like crystals. The product was characterized by 1H NMR (CDCl3): δ 10.45 (s, 1H), 8.70 (d, J = 2.9Hz, 1H), 8.45 (dd, J = 8.8, 2.9Hz, 1H), 7.14 (d, J = 8.8Hz, 1H), 4.08 (s, 3H). | [References]
[1] Angewandte Chemie - International Edition, 2011, vol. 50, # 15, p. 3435 - 3438 [2] Patent: US2013/261295, 2013, A1. Location in patent: Paragraph 0166; 0167 [3] Journal of the American Chemical Society, 2017, vol. 139, # 19, p. 6654 - 6662 [4] Patent: US5837711, 1998, A [5] Journal of the Chemical Society, 1951, p. 2462,2466 |
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Energy Chemical
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