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Chemical Structure| 866588-11-6 Chemical Structure| 866588-11-6

Structure of 866588-11-6

Chemical Structure| 866588-11-6

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Product Details of [ 866588-11-6 ]

CAS No. :866588-11-6
Formula : C12H11FN2O2
M.W : 234.23
SMILES Code : O=C(C1=CC(C2=CC=C(F)C=C2)=NN1)OCC
MDL No. :MFCD08445938

Safety of [ 866588-11-6 ]

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 [ 866588-11-6 ]

* 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 [ 866588-11-6 ]

[ 866588-11-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 31686-94-9 ]
  • [ 866588-11-6 ]
YieldReaction ConditionsOperation in experiment
100% With hydrazine; In ethanol; for 1h;Heating / reflux; A mixture of <strong>[31686-94-9]ethyl 3-(4-fluorobenzoyl)pyruvate</strong> (11.3 g, 47.4 mmol), hydrazine monohydrate (2.50 g, 50.0 mmol) and ethanol (50 mL) was heated under reflux for 1 hr. The reaction mixture was cooled and poured into water. The precipitated solid was collected by filtration, washed with water, and dried to give the title compound (11.0 g, quantitative) as colorless crystals. 1H NMR (CDCl3) delta: 1.41(3H, t, J=7.2Hz), 4.41(2H, q, J=7.2Hz), 7.05-7.18(3H, m), 7.76(2H, dd, J=8.2, 5.4Hz), 11.21(1 H, s).
67% With hydrazine hydrate; In ethanol; for 1h;Reflux; To a solution of Intermediate 1A (120 g, 504 mmol) in ethanol (1200 mL) was added hydrazine monohydrate (25.7 mL, 529 mmol) slowly and the resulting reaction mixture was refluxed for 1 h. Reaction mixture was cooled to RT, poured into ice cold water, and the resultant solid dried under vacuum to afford Intermediate 1B (80 g, 67%). MS(ES): m/z=235 [M+H]+; 1H NMR (300 MHz, CDCl3) delta ppm 7.75 (m, 2H), 7.12 (m, 2H), 7.07 (s, 1H), 4.42 (q, J=7.2 Hz, 2H), 1.42 (t, J=7.2 Hz, 3H).
80 g With hydrazine hydrate; In ethanol; for 1h;Reflux; To a solution of Intermediate 1 A (120 g, 504 mmol) in ethanol (1200 mL) was added hydrazine monohydrate (25.7 mL, 529 mmol) slowly and the resulting reaction mixture was refluxed for 1 h. The reaction mixture was cooled to RT, poured into ice cold water and the resultant solid was filtered and dried under vacuum to afford (0371) Intermediate IB (80 g, 67%). MS(ES): m/z = 235 [M+H]+; 1H NMR (300 MHz, CDC13) delta ppm 7.75 (m, 2H), 7.12 (m, 2H), 7.07 (s, 1H), 4.42 (q, J= 7.2 Hz, 2H), 1.42 (t, J= 7.2 Hz, 3H)
With hydrazine hydrate; acetic acid; In ethanol; at 90℃; for 3h; General procedure: Weigh 0.1 mol (1 eq) of the intermediate compound? -diketate 2 in a 250 ml round bottom flask,6.3 g (1 eq) of 80% hydrazine hydrate was added,Add 100ml of anhydrous ethanol and 1ml of glacial acetic acid,90 C for 3 hours,TLC detection without intermediate 2, the reaction completed.System vacuum distillation solvent,A white yellowish solid.The solid is transferred to water,Stir,filter,dry,A white solid.
16.8 g With hydrazine dihydrochloride; In ethanol; for 3h;Reflux; General procedure: To a stirred solution of appropriate methyl ketone (0.1 mol) in dry toluene (200 mL)was added a suspension of NaH in mineral oil (60%; 0.2 mol) in portions and the mixture was warmed to50 C. At this temperature a solution of diethyl oxalate (0.15 mol) in dry toluene (60 mL) was addeddropwise under stirring. The reaction mixture was refluxed for 1.5 h. Upon cooling to room temperatureacetic acid (0.25 mol) was added dropwise. The reaction mixture was washed with water (200 mL), organicphase was dried over MgSO4 and evaporated to dryness. The obtained crude diketone was dissolved inethanol (250 mL), hydrazine dihydrochloride (0.11 mol) was added and the mixture was refluxed for 3 h.After evaporation of solvent the residue was treated with water (200 mL) and kept under ice-cooling for 1 h.Crystals were filtered off and dried in air to afford the corresponding pyrazole. In some cases thus obtainedsubstance was purified by recrystallization from aqueous ethanol.

  • 2
  • [ 31686-94-9 ]
  • [ 866588-11-6 ]
YieldReaction ConditionsOperation in experiment
58% With hydrogenchloride; hydrazine hydrate; In ethanol; water; at 20℃; Example 56 Ethyl 5-(4-fluorophenyl)-1H-pyrazole-3-carboxylate To a solution of <strong>[31686-94-9]ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate</strong> (512 mg, 2.15 mmol) in ethanol (7 mL) was slowly added hydrazine monohydrate (0.14 mL, 2.15 mmol). Following the addition of 1M HCl 0.1 mL thereto, the reaction mixture was stirred overnight at room temperature. When the reaction was completed as monitored by TLC (Hexane:EtOAc=4:1), the reaction mixture was concentrated in vacuo. After extraction with dichloromethane and water, the organic layer thus formed was dried over anhydrous magnesium sulfate, filtered, and concentrated. The concentrated filtrate was recrystallized in dichloromethane, and purified by column chromatography (Hexane:EtOAc=4:1?CH2Cl2:MeOH=12:1) to afford the title compound (290 mg, 58%, yellow solid). 1H NMR (300 MHz, CDCl3) delta 7.78 (brs, 2H), 7.18-7.14 (m, 2H), 7.11 (s, 1H), 4.46 (q, J=7.0, 2H), 1.45 (t, J=7.0 Hz, 3H)
 

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