| Identification | Back Directory | [Name]
4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACID | [CAS]
60547-92-4 | [Synonyms]
2-(Benzyloxy)-5-carboxy-4-nitroansole
4-Benzyloxy-3-Methoxy-6-nitrobenzoic acid
4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACID
2-Nitro-4-(benzyloxy)-5-methoxybenzoic acid
5-Methoxy-2-nitro-4-(phenylMethyloxy)benzoic acid
Benzoic acid, 5-Methoxy-2-nitro-4-(phenylMethoxy)-
2-(Benzyloxy)-5-carboxy-4-nitroansole, 5-(Benzyloxy)-2-carboxy-4-methoxynitroben
2-(Benzyloxy)-5-carboxy-4-nitroansole, 5-(Benzyloxy)-2-carboxy-4-methoxynitrobenzene | [Molecular Formula]
C15H13NO6 | [MDL Number]
MFCD04114356 | [MOL File]
60547-92-4.mol | [Molecular Weight]
303.27 |
| Chemical Properties | Back Directory | [Melting point ]
192 °C | [Boiling point ]
504.4±50.0 °C(Predicted) | [density ]
1.362±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
2.34±0.25(Predicted) | [Appearance]
White to off-white Solid | [InChI]
InChI=1S/C15H13NO6/c1-21-13-7-11(15(17)18)12(16(19)20)8-14(13)22-9-10-5-3-2-4-6-10/h2-8H,9H2,1H3,(H,17,18) | [InChIKey]
VTHHRADLOLKTLD-UHFFFAOYSA-N | [SMILES]
C(O)(=O)C1=CC(OC)=C(OCC2=CC=CC=C2)C=C1[N+]([O-])=O |
| Hazard Information | Back Directory | [Uses]
4-?(Benzyloxy)?-?5-?methoxy-?2-?nitrobenzoic Acid is a reagent used in the preparation of benzodiazepine-based β-glucoside prodrugs for use in cancer chemotherapy. | [Synthesis]
General procedure for the synthesis of 2-nitro-4-benzyloxy-5-methoxybenzoic acid from 4-(benzyloxy)-5-methoxy-2-nitrobenzaldehyde: 4-(benzyloxy)-5-methoxy-2-nitrobenzaldehyde (20 g, 69.62 mmol) was dissolved in acetone (200 mL), and preheated 10% potassium permanganate solution was added slowly at 30 °C. The reaction mixture was stirred at 50 °C for 2 h and then cooled to room temperature. Subsequently, the mixture was filtered through a diatomaceous earth pad and the filter cake was washed with acetone and a little hot water. The filtrate was concentrated under reduced pressure and cooled to 0°C. The concentrate was acidified to pH 4 with hydrochloric acid, stirred for 30 min and filtered to give a solid product of 2-nitro-4-benzyloxy-5-methoxybenzoic acid (18.5 g, 88% yield). The product was confirmed by NMR hydrogen spectrum (300 MHz, DMSO-d6): δ 13.58 (brs, 1H), 7.70 (s, 1H), 7.46-7.40 (m, 6H), 7.39 (s, 1H), 5.25 (s, 2H), 3.92 (s, 3H). Mass spectrum (ESI+, m/z): 304 [M+H]+. | [References]
[1] Patent: WO2012/30160, 2012, A2. Location in patent: Page/Page column 50
[2] Patent: WO2017/194960, 2017, A1. Location in patent: Page/Page column 187
[3] Patent: US4950674, 1990, A
[4] Farmaco, Edizione Scientifica, 1977, vol. 32, # 8, p. 579 - 591
[5] Tetrahedron Letters, 1986, vol. 27, # 10, p. 1149 - 1152 |
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