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Chemical Structure| 1874-23-3 Chemical Structure| 1874-23-3

Structure of 1874-23-3

Chemical Structure| 1874-23-3

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Product Details of [ 1874-23-3 ]

CAS No. :1874-23-3
Formula : C6H5NO5
M.W : 171.11
SMILES Code : O=C(C1=CC=C([N+]([O-])=O)O1)OC
MDL No. :MFCD00051956
InChI Key :UTLKCGPAJUYGOM-UHFFFAOYSA-N
Pubchem ID :94882

Safety of [ 1874-23-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 1874-23-3 ]

* 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 [ 1874-23-3 ]

[ 1874-23-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1874-23-3 ]
  • [ 824-38-4 ]
  • [ 2217-65-4 ]
  • 2
  • [ 1874-23-3 ]
  • [ 22600-30-2 ]
YieldReaction ConditionsOperation in experiment
With hydrogen;palladium 10% on activated carbon; In ethyl acetate; at 20℃; under 760.051 Torr; for 2h; A solution of 100 mg of methyl 5-nitro-2-furoate (Lancaster Synthesis, Windham, N.H., USA) in 20 ml of EtOAc was stirred with 20 mg of Pd/C (10%) under one atmospheric pressure of hydrogen gas. After at RT for 2 hours, the mixture was filtered through a celite pad and concentrated. Pure methyl 5-amino-2-furoate was obtained by purification on a fresh silica gel column eluted with 30% EtOAc in hexane.
4.03 g With palladium 10% on activated carbon; hydrogen; In ethanol; at 20℃; for 18h; Pd/C 10% wet (2.5 g) was added to a solution of methyl-5-nitrofuran-2-carboxylate (5 g, 29.2 mmol) in EtOH (50 mL) and the reaction mixture was hydrogenated at rt for 18h under atmospheric pressure. Then the catalyst was filtered off and the filtrate concentrated in vacuum to give a dark red solid (4.03 g, 28.6 mmol). LC (Method F): 1.059 min. LCMS: Anal. Calcd. for C6H7NO3: 141.02, found: 142.04 (M+1)+; 1H NMR (600 MHz, CDCl3) δ ppm 7.03 (d, J= 3.6Hz, 1H), 5.20 (d, J=3.6Hz, 1H), 4.55 (sb, 2H), 3.75 (s, 3H).
With palladium 10% on activated carbon; hydrogen; In methanol; at 20℃; for 2h; Dissolve 4-18 (171mg, 1mmol) in methanol (10mL), add Pd/C (10%, 17mg),Place in a hydrogenator to react at room temperature for 2 hours, and TLC (PE:EA=3:1) detects that the reaction is complete.The reaction solution was filtered through Celite, and the filtrate was concentrated to obtain a yellow oil (3-27).
 

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