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Methyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate

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Methyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate Basic information

Product Name:
Methyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate
Synonyms:
  • Methyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate
  • 4-Benzyloxy-5-methoxy-2-nitrobenzoic acid methyl ester
  • Methyl 5-methoxy-2-nitro-4-(benzyloxy)benzoate
  • ethyl 4-(benzyloxy)-5-Methoxy-2-nitrobenzoate
  • Benzoic acid, 5-Methoxy-2-nitro-4-(phenylMethoxy)-, Methyl ester
  • methyl 5-methoxy-2-nitro-4-phenylmethoxybenzoate
CAS:
61032-41-5
MF:
C16H15NO6
MW:
317.29
Mol File:
61032-41-5.mol
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Methyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate Chemical Properties

Boiling point:
482.4±40.0 °C(Predicted)
Density 
1.280
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
InChI
InChI=1S/C16H15NO6/c1-21-14-8-12(16(18)22-2)13(17(19)20)9-15(14)23-10-11-6-4-3-5-7-11/h3-9H,10H2,1-2H3
InChIKey
GUOGVJFNFLXSLK-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC(OC)=C(OCC2=CC=CC=C2)C=C1[N+]([O-])=O
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Methyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate Usage And Synthesis

Synthesis

56441-97-5

61032-41-5

4.1.4 Synthesis of methyl 4-benzyloxy-5-methoxy-2-nitrobenzoate (12): intermediate 11 (10.1 g, 37 mmol) was suspended in acetic acid (100 mL) and 70% nitric acid (20 mL) was added slowly. Subsequently, the reaction mixture was heated to 50 °C and maintained at this temperature for 5 hours. Upon completion of the reaction, the mixture was cooled to room temperature and poured into ice water (500 mL). After stirring for 1 hour, the precipitate precipitated was collected by filtration, washed with water and dried to give nitro compound 12 as a white solid. Yield: 86%, melting point: 126-128°C.

References

[1] Patent: WO2016/148674, 2016, A1. Location in patent: Page/Page column 114
[2] Patent: US2009/76044, 2009, A1. Location in patent: Page/Page column 26
[3] Patent: US2017/95570, 2017, A1. Location in patent: Paragraph 0571; 0573
[4] Patent: US2014/235634, 2014, A1. Location in patent: Paragraph 0390; 0392
[5] Asian Journal of Chemistry, 2015, vol. 27, # 7, p. 2647 - 2650

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