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Chemical Structure| 145742-68-3 Chemical Structure| 145742-68-3

Structure of 145742-68-3

Chemical Structure| 145742-68-3

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Product Details of [ 145742-68-3 ]

CAS No. :145742-68-3
Formula : C8H5ClF2O2
M.W : 206.57
SMILES Code : O=CC1=CC(Cl)=CC=C1OC(F)F
MDL No. :MFCD03412195

Safety of [ 145742-68-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P301+P312+P330

Application In Synthesis of [ 145742-68-3 ]

* 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 [ 145742-68-3 ]

[ 145742-68-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 145742-68-3 ]
  • [ 62327-21-3 ]
  • [ 1329166-86-0 ]
YieldReaction ConditionsOperation in experiment
74% With potassium tert-butylate; In tetrahydrofuran; at 0 - 20℃; for 4h; To a cooled (0 °C) solution of potassium tert-butoxide (0.407 g, 3.63 mmol) in THF (10 mL) was added tert-butyl 2-(dimethoxyphosphoryl)acetate (0.528 mL, 2.66 mmol) and 5-chloro-2-(difluoromethoxy)benzaldehyde (0.50g, 2.420 mmol). The reaction was allowed to warm to RT. After 4h, the reaction was quenched with the addition of sat. ammonium chloride. The reaction was diluted with EtOAc, washed with sat. ammonium chloride, sat NaHCC^ and brine. The organic layer was dried over sodium sulfate, filtered and concentrated. Purification by normal phase chromatography gave 550 mg (74percent) of Intermediate 24A as a white solid. NMR (400 MHz, CDC13) delta ppm 7.77 (1 H, d, J=16.31 Hz), 7.58 (1 H, d, J=2.51 Hz), 7.31 (1 H, dd, J=8.66, 2.64 Hz), 7.12 (1 H, d, J=8.78 Hz), 6.52 (1 H, t, J=72.78 Hz) 6.40 (1 H, d, J=16.31 Hz), 1.53 (9 H, s). 19F NMR (376 MHz, CDC13) delta ppm -81.11. MS (ESI) m/z: 327.0 (M+Na)+.
74% With potassium tert-butylate; In tetrahydrofuran; at 0℃; for 4h; To a solution of potassium tert-butoxide (0.407 g, 3.63 mmol) in THF (10 mL) were added tert-butyl 2-(dimethoxyphosphoryl)acetate (0.528 mL, 2.66 mmol) and 5- chloro-2-(difluoromethoxy)benzaldehyde (0.50 g, 2.420 mmol) at 0 °C. After 4 h, NH4Cl solution was added and the reaction mixture was diluted with EtOAc, washed with saturated NH4Cl solution, saturated NaHCO3, and brine. The organic phase was dried over Na2SO4, filtered and concentrated. The crude product was purified by normal phase chromatography to yield Intermediate 15A as a white solid (550 mg, 74percent). MS (ESI) m/z: 327.0 (M+Na)+. 19F NMR (376 MHz, CDCl3) delta -81.1 1 (1 F, s) ppm
74% With potassium tert-butylate; In tetrahydrofuran; at 0℃; for 4h; To a solution of potassium tert-butoxide (0.407 g, 3.63 mmol) in THF (10 mL) were added tert-butyl 2-(dimethoxyphosphoryl)acetate (0.528 mL, 2.66 mmol) and 5- chloro-2-(difluoromethoxy)benzaldehyde (0.50 g, 2.420 mmol) at 0 °C. After 4 hrs, NH4Cl solution was added and the reaction mixture was diluted with EtOAc, washed with sat'd NH4Cl solution, sat'd NaHCO3 , and brine. The organic phase was dried over Na2S04, filtered and concentrated. The crude product was purified by normal phase chromatography. Intermediate 15A was obtained as a white solid 550 mg (74percent). MS (ESI) m/z: 327.0 (M+Na)+.19F NMR (376 MHz, CDC13) delta: -81.1 1 (1 F, s) ppm.
74% With potassium tert-butylate; In tetrahydrofuran; at 0℃; for 4h; To a solution of potassium fert-butoxide (0.407 g, 3.63 mmol) in THF (10 mL) were added tert-butyl 2-(dimethoxyphosphoryl)acetate (0.528 mL, 2.66 mmol) and 5- chloro-2-(difluoromethoxy)benzaldehyde (0.50 g, 2.420 mmol) at 0 °C. After 4 hrs, NH4Cl solution was added and the reaction mixture was diluted with EtOAc, washed with sat'd NH4Cl solution, sat'd NaHCO3 and brine. The organic phase was dried over Na2SO4, filtered and concentrated. The crude product was purified by normal phase chromatography. Intermediate 15A was obtained as a white solid 550 mg (74percent). MS (ESI) m/z: 327.0 (M+Na)+.19F NMR (376 MHz, CDCl3) delta: -81.11 (1 F, s) ppm

 

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• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Julia-Kocienski Olefination • Kinetics of Alkyl Halides • Knoevenagel Condensation • Kumada Cross-Coupling Reaction • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nomenclature of Ethers • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Ethers • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Ethers • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Stetter Reaction • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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