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Chemical Structure| 640291-92-5 Chemical Structure| 640291-92-5

Structure of 640291-92-5

Chemical Structure| 640291-92-5

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Product Details of [ 640291-92-5 ]

CAS No. :640291-92-5
Formula : C12H10FNO3
M.W : 235.21
SMILES Code : O=C(C1=CC(C2=CC=C(F)C=C2)=NO1)OCC
MDL No. :MFCD08446405

Safety of [ 640291-92-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of [ 640291-92-5 ]

* 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 [ 640291-92-5 ]

[ 640291-92-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 31686-94-9 ]
  • [ 640291-92-5 ]
YieldReaction ConditionsOperation in experiment
26% With hydroxylamine hydrochloride; In ethanol; at 90℃; NH2OHHC1 (2.92 g, 5.00 eq.) was added to a solution of <strong>[31686-94-9]ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate</strong> (2 g, 8.40 mmol, 1.00 eq.) in ethanol (20 mL). The resulting solution was stirred overnight at 90 C in anoil bath. The solids were filtered and the resulting mixture was concentrated under vacuum.The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:25).This resulted in 518 mg (26%) of ethyl 5-(4-fluorophenyl)isoxazole-3-carboxylate as a whitesolid. ?HNMR(400MHz, CDC13): oe 7.85-7.81 (m, 2H), 7.23-7.19 (m, 2H), 6.90 (s, 1H), 4.53-4.47 (m, 2H), 1.49-1.45 (t, J= 7.2 Hz, 3H).
26% With hydroxylamine hydrochloride; In ethanol; at 90℃; NH2OH HCl (2 92 g, 5.00 eq.) was added to a solution of <strong>[31686-94-9]ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate</strong> (2 g, 8.40 mmol, 1.00 eq.) in ethanol (20 mL). The resulting solution was stirred overnight at 90 C in an oil bath. The solids were filtered and the resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1 :25). This resulted in 518 mg (26%) of ethyl 5-(4-fluorophenyl)isoxazole-3-carboxylate as a white solid. NMR (400MHz, CDC13): delta 7.85-7.81 (m, 2H), 7.23-7.19 (m, 2H), 6.90 (s, 1H), 4.53- 4.47 (m, 2H), 1.49-1.45 (t, J= 7.2 Hz, 3H).
24 g With hydroxylamine hydrochloride; In ethanol; at 0 - 80℃; for 3h; To a stirred solution of ethyl 4-(4- fluorophenyl)-2,4-dioxobutanoate (44.0 g, 187mmol) in ethanol (600mL) at 0 C, was added hydroxyl amine hydrochloride (39.0 g, 561mmol) portion wise at 0 C. The reaction mixture was then stirred at 80 C for 3h. The reaction mixture was concentrated under reduce pressure and the resulting residue was suspended in water (500mL). The precipitates were collected by filtration and dried under vacuum to give crude product which was purified by column chromatography (eluted in 0-15% Ethyl acetate in Hexane) to obtained ethyl 5-(4- fluorophenyl)isoxazole-3-carboxylate (24.0 g, 236 [M+H]). 1H NMR: (400 MHz, DMSO) delta: 1.601-1.610 (t, 3H), 4.468-4.530 (m, 2H), 6.898-6.908 (t,lH), 7.188-7.230 (m, 2H), 7.810-7.849 (m, 2H).
With hydroxylamine hydrochloride; In methanol;Reflux; A mixture of 20 (3 g, 11.03 mmol) and NH2eOH.HCl (2.28 g,33.09 mmol) in MeOH (50 mL) was heated to reflux overnight. TheMeOH was then evaporated and the residue was extracted withethyl acetate, dried over Na2SO4. After filtration and concentrationin vacuo, the crude residue was purified by column to afford 21; MS(ESI)m/z (%): 236.1 [M H]; 1H NMR (400 MHz, CDCl3) d7.85e7.78(m, 2H), 7.20 (t, J 8.6 Hz, 2H), 6.89 (s, 1H), 4.01 (s, 3H).

 

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