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[ CAS No. 79538-27-5 ] {[proInfo.proName]}

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Chemical Structure| 79538-27-5
Chemical Structure| 79538-27-5
Structure of 79538-27-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 79538-27-5 ]

CAS No. :79538-27-5 MDL No. :MFCD04115923
Formula : C8H8F2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 174.15 Pubchem ID :-
Synonyms :

Safety of [ 79538-27-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 79538-27-5 ]

* 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 [ 79538-27-5 ]

[ 79538-27-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 79538-27-5 ]
  • [ 94278-68-9 ]
YieldReaction ConditionsOperation in experiment
66% With phosphorus(V) oxybromide In tetrahydrofuran at 20℃; for 2h; 56.3 Step3: Step3: To a cold stirring solution of (2,6-difluoro-4-methoxyphenyl)MeOH (0.5 g, 2.87 mmol, 1 eq) in THF (20 ml) was portion wise added ROB FontWeight="Bold" FontSize="10" (1.65 g, 5.74 mmol, 2 eq). The reaction mixture then stirred for 2 h at RT. The reaction mixture was quenched by saturated NaHCCb solution under cooling conditions. The organic layer was separated and aqueous layer was extracted by EtOAc (50 ml). The combined organic layer was washed by water (30 ml) and brine (30 ml). [71] The organic layer was dried over anhydrous Na2SC>4, concentrated under reduced pressure to get the crude material which was purified by silica gel (230-400 mesh silica gel; 10% EtO Ac/hexane; R value-0.5) to afford 2-(bromomethyl)-1,3-difluoro-5-methoxybenzene (0.45 g, 66%) as color less liquid.
With hydrogen bromide; acetic acid for 0.75h; Heating;
  • 2
  • [ 84937-82-6 ]
  • [ 79538-27-5 ]
  • 3
  • [ 79538-28-6 ]
  • [ 79538-27-5 ]
  • 4
  • [ 256417-10-4 ]
  • [ 79538-27-5 ]
YieldReaction ConditionsOperation in experiment
95% With sodium tetrahydroborate; In methanol; at 20℃; for 1h; Step2: To a cold stirring solution of <strong>[256417-10-4]2,6-difluoro-4-methoxybenzaldehyde</strong> (2.3 g, 13.37 mmol, 1 eq) in MeOH (68 ml) was portion wise added NaBFE (0.65 g, 17.11 mmol, 1.28 eq). The reaction mixture was then stirred for 1 h at RT. The reaction mixture was then quenched by addition of ice (10 g). The solvents were evaporated and the residue was dissolved in EtOAc (100 ml) and washed by water (2 x 50 ml) followed by brine (100 ml). The organic layer was dried over anhydrous Na2S04, concentrated under reduced pressure to get (2,6-difluoro-4-methoxyphenyl)MeOH (2.2 g, 95%) as off white solid.
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