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Chemical Structure| 1240286-88-7 Chemical Structure| 1240286-88-7

Structure of 1240286-88-7

Chemical Structure| 1240286-88-7

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Product Details of [ 1240286-88-7 ]

CAS No. :1240286-88-7
Formula : C8H8BrFO3S
M.W : 283.11
SMILES Code : CS(=O)(OCC1=CC=C(Br)C(F)=C1)=O
MDL No. :MFCD26403892

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Application In Synthesis of [ 1240286-88-7 ]

* 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 [ 1240286-88-7 ]

[ 1240286-88-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 124-63-0 ]
  • [ 222978-01-0 ]
  • [ 1240286-88-7 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; at 0 - 20℃; A cooled (0 0C) solution of <strong>[222978-01-0](4-bromo-3-fluorophenyl)methanol</strong> (Intermediate 9; 299 mg; 1.46 mmol) and methanesulfonyl chloride (147 muL; 1.90 mmol) in DCM (3 mL) was treated slowly with a solution of triethylamine (305 muL; 2.19 mmol) in DCM (1.5 mL). The reaction mixture was allowed to warm to RT and stirred for 45 minutes before being quenched by addition of water. The organic phase was washed with HCI (0.1 N in water) and brine, dried over MgSO4, filtered and concentrated to dryness affording a residue, which was purified by flash column chromatography, eluting with cyclohexane containing increasing amounts of EtOAc to give the title compound as a colourless liquid.1H NMR (300MHz, DMSO-d6) delta [ppm] 7.77 (1 H, dd, J= 8.2, J= 7.5 Hz), 7.48 (1 H, dd, J= 9.7, J= 2.0 Hz), 7.26 (1 H, dd, J= 8.2, J= 2.0 Hz), 5.26 (2H, s), 3.27 (3H, s).
With sodium hydrogencarbonate; triethylamine; In dichloromethane; water; Reference Example 66 4-Bromo-3-fluorobenzyl methanesulfonate A solution of the compound (30.0 g) obtained in Reference Example 65 and triethylamine (22.4 mL) in dichloromethane (300 mL) was cooled to 0 C. Methanesulfonyl chloride (12.5 mL) was added dropwise thereto, and the mixture was stirred at the same temperature as above for 1.5 hours. The reaction mixture was washed with a mixed solution of a saturated aqueous solution of sodium bicarbonate and water (1:3) (300 mL) and saturated aqueous sodium chloride (300 mL), dried over anhydrous sodium sulfate, and then concentrated to obtain the title compound (40.7 g). 1H NMR (CDCl3, 400 MHz): delta (ppm) 7.57-7.62 (m, 1H), 7.18-7.22 (m, 1H), 7.07-7.11 (m, 1H), 5.18 (s, 2H), 3.00 (s, 3H)
With triethylamine; In dichloromethane; at -78 - 0℃; for 1h; Step 5: Preparation of (4-bromo-3-fluorophenyl')acetonitrile; To a -78C solution of <strong>[222978-01-0](4-bromo-3-fluorophenyl)methanol</strong> from Step 4 (7.2 g) and triethylamine (5.9 mL) in dichloromethane (300 mL) was slowly added methanesulphonyl chloride (3.0 mL) The reaction mixture was stirred at 00C for 1 hour and then poured into ice and saturated aqueous ammonium chloride and partitioned. T he aqueous layer was extracted with dichloromethane (1 x 150 mL) The combined extracts were washed with brine, dried with magnesium sulfate and the solvent removed in vacuo. The residue was dissolved in DMF (150 mL) and sodium cyanide (5.1 g) was added. The reaction mixture was stirred at room temperature for 2 hours and poured into ice and water (100 mL) The aqueous phase was extracted with ethyl acetate (2 x 100 mL). The combined organic extracts were washed with brine, dried with magnesium sulfate and the solvent removed in vacuo. The residue was purified by chromatography on SiO2 using ethyl acetate and hexanes (1: 10 to 1:5) to yield the title compound.1H NMR (CD3COCD3) delta 7.70-7.78 (1 H, m), 7.39 (1 H, d), 7.28 (1 H, d), 4.09 (2 H, s).
 

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