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Chemical Structure| 214472-37-4 Chemical Structure| 214472-37-4

Structure of 214472-37-4

Chemical Structure| 214472-37-4

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Product Details of [ 214472-37-4 ]

CAS No. :214472-37-4
Formula : C16H22N2O7
M.W : 354.36
SMILES Code : O=C(OC)C1=CC(OCCCN2CCOCC2)=C(OC)C=C1[N+]([O-])=O
MDL No. :MFCD26743437

Safety of [ 214472-37-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 214472-37-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 214472-37-4 ]

[ 214472-37-4 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 215659-03-3 ]
  • [ 57616-74-7 ]
  • [ 214472-37-4 ]
YieldReaction ConditionsOperation in experiment
87.5% With potassium carbonate; In acetonitrile; for 2.5h;Reflux; To a slurry of compound 2 (10.0 g, 0.044 mol) and anhydrous potassium carbonate (18.2 g, 0.1317 mol) in acetonitrile (100 ml), <strong>[57616-74-7]4-<strong>[57616-74-7](3-chloropropyl)morpholine hydrochloride</strong></strong> (10 g, 0.05 mol) was added and refluxed for 2.5 h. The solvent was distilled under reduced pressure to give residue which was diluted with water(60 ml) and extracted with ethyl acetate (100 ml) after completion of reaction. The organic layer was distilled under vacuum and dried to obtain 13.65 g (87.50%) of the compound 3; m. p. 231-233 C. 1HNMR (DMSO-d6, 400 MHz): delta 7.62 (s, 1H), 7.31 (s, 1H), 7.07 (s, 1H),3.90 (s, 3H), 3.79 (s, 3H), 4.18 (t, 2H), 4.17 (s, 2H), 4.16 (s, 3H), 2.37 (d,1H), 1.91 (d, 2H). IR (numax, cm-1): 3134, 1695, 1601.
With potassium carbonate; In acetonitrile; for 2.5h;Reflux; Example 6; Preparation of 4-methoxy-5-(3-morpholin-4-ylpropoxy)-2-nitro benzoic acid methyl ester; To a mixture of 5-hydroxy-4-methoxy-2-nitrobenzoic acid methyl ester (10 g) and anhydrous potassium carbonate (18.2 g) in acetonitrile (100 ml), <strong>[57616-74-7]4-(3-chloropropyl)-morpholine hydrochloride</strong> (10 g) was added and refluxed for 2.5 hours. After completion of reaction, the solvent was distilled under reduced pressure to give residue which was diluted with water and extracted with ethyl acetate. The organic layer was distilled under vacuum and dried to obtain 14 g of the title compound.
 

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