Home Cart Sign in  
Chemical Structure| 1079352-13-8 Chemical Structure| 1079352-13-8

Structure of 1079352-13-8

Chemical Structure| 1079352-13-8

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 1079352-13-8 ]

CAS No. :1079352-13-8
Formula : C7H6BrF2NO
M.W : 238.03
SMILES Code : CC1=CC(OC(F)F)=NC=C1Br
MDL No. :MFCD14698387

Safety of [ 1079352-13-8 ]

Application In Synthesis of [ 1079352-13-8 ]

* 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 [ 1079352-13-8 ]

[ 1079352-13-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 75-45-6 ]
  • [ 164513-38-6 ]
  • [ 1079352-13-8 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In tetrahydrofuran; water; at 70℃; 5N aqueous solution of sodium hydroxide (5.70 mL) was added to the tetrahydrofuran solution (28 mL) of <strong>[164513-38-6]5-bromo-2-hydroxy-4-methylpyridine</strong> (1.07 g). The reaction mixture was stirred at 70C under chlorodifluoromethane gas atmosphere. The reaction mixture was cooled to room temperature after the disappearance of raw material, diluted with tert-butyl methyl ether, and extracted. The organic layer was washed by water and a saturated aqueous solution of sodium chloride, and dried with magnesium sulfate. The organic layer was concentrated under reduced pressure. The obtained residue was purified by column chromatography on silica gel (high flash-SI, size L (made in Yamazen corporation)) to obtain a title compound (751 mg) having the following physical data. TLC:Rf 0.58 (ethyl acetate/n-hexane=5/95); 1H-NMR(CDCl3): δ 2.40 (d, J=0.7 Hz, 3 H), 6.80 (s, 1 H), 7.39 (t, J=72.9 Hz, 1 H), 8.22 (s, 1 H).
  • 2
  • [ 1717-59-5 ]
  • [ 164513-38-6 ]
  • [ 1079352-13-8 ]
YieldReaction ConditionsOperation in experiment
37% With sodium sulfate; In acetonitrile; at 20℃; 5-Bromo-2-(difluoromethoxy)-4-methylpyridine (B11.1) (0385) To a solution of <strong>[164513-38-6]5-bromo-4-methylpyridin-2-ol</strong> (8 g, 42.55 mmol) and 2,2-difluoro-2-(fluorosulfonyl)acetic acid (9.1 g, 51.06 mmol) in 40 mL CH3CN was added Na2SO4 (606 mg, 4.255 mmol) in one portion. The suspension was stirred at rt overnight, then concentrated under vacuum, the residue was purified on silica gel (PE/EtOAc=0-9%) to give the title compound (500 mg, 37%) as a yellow oil. 1H NMR (500 MHz, DMSO-d6) b 2.39 (s, 3H), 7.19 (s, 1H), 7.51-7.80 (m, 1H), 8.39 (s, 1H). LC-MS: [M+H]+=239.9.
37% With sodium sulfate; In acetonitrile; at 20℃; To a solution of 5- bromo-4-methylpyridin-2-ol (8 g, 42.55 mmol) and 2 ,2-difluoro-2-(fluorosulfonyl)acetic acid (9.1 g, 51.06 mmol) in 40 mL CH3CN was added Na2SO4 (606 mg, 4.255 mmol) inone portion. The suspension was stirred at rt overnight, then concentrated under vacuum, the residue was purified on silica gel (PE/EtOAc = 0- 9 %) to give the title compound (500 mg, 37%) as a yellow oil. 1H NMR (500 MHz, DMSO-d6) O 2.39 (5, 3H), 7.19 (5, 1H), 7.51-7.80 (m, 1H), 8.39 (5, 1H). LC-MS: [M+H] = 239.9.
 

Historical Records