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[ CAS No. 1325694-78-7 ] {[proInfo.proName]}

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Chemical Structure| 1325694-78-7
Chemical Structure| 1325694-78-7
Structure of 1325694-78-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1325694-78-7 ]

CAS No. :1325694-78-7 MDL No. :
Formula : C12H10BrClN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :KLFCDTDRDRISSC-UHFFFAOYSA-N
M.W : 329.58 Pubchem ID :84819521
Synonyms :

Safety of [ 1325694-78-7 ]

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 [ 1325694-78-7 ]

* 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.

  • Upstream synthesis route of [ 1325694-78-7 ]
  • Downstream synthetic route of [ 1325694-78-7 ]

[ 1325694-78-7 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 68797-61-5 ]
  • [ 105-13-5 ]
  • [ 1325694-78-7 ]
YieldReaction ConditionsOperation in experiment
33% With potassium <i>tert</i>-butylate In tetrahydrofuran at 50℃; for 16 h; Inert atmosphere General procedure: To a mixture of dichloride 21 (0.625 g, 2.7 mmol) and potassium tert-butoxide (0.395 g, 4.1 mmol) was added a solution of para-methoxybenzyl alcohol (0.568 g, 4.1 mmol) in THF (8 mL). Reaction mixture was heated to 50 °C overnight. Reaction mixture was filtered and concentrated under reduced pressure. Product was purified via automated chromatography (EtOAc: Hexanes, 20:80) to provide 22 as a clear oil in 33percent yield. 1H NMR (400 MHz, CDCl3) δ 8.38 (s, 1H), 7.30 (d, J = 8.6 Hz, 1H), 6.83 (d, J = 8.6 Hz, 1H), 5.38 (s, 2H), 3.73 (s, 3H). 13C NMR (101 MHz, CDCl3) δ 166.68, 160.23, 159.85, 155.22, 130.28, 130.16, 130.00, 127.24, 114.02, 106.27, 70.10, 55.32.
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 15, p. 4592 - 4596
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