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Chemical Structure| 834-14-0 Chemical Structure| 834-14-0

Structure of 4-MDM
CAS No.: 834-14-0

Chemical Structure| 834-14-0

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Synonyms: 4-Methoxydiphenylmethane

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Product Details of [ 834-14-0 ]

CAS No. :834-14-0
Formula : C14H14O
M.W : 198.26
SMILES Code : COC1=CC=C(CC2=CC=CC=C2)C=C1
Synonyms :
4-Methoxydiphenylmethane
MDL No. :MFCD00094072
InChI Key :GQLYCRTUQGSDSM-UHFFFAOYSA-N
Pubchem ID :13264

Safety of [ 834-14-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H315-H318-H400
Precautionary Statements:P273-P280-P305+P351+P338
Class:9
UN#:3082
Packing Group:

Application In Synthesis of [ 834-14-0 ]

* 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 [ 834-14-0 ]

[ 834-14-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 104-21-2 ]
  • [ 98-80-6 ]
  • [ 834-14-0 ]
  • 2
  • [ 5720-07-0 ]
  • [ 5350-41-4 ]
  • [ 834-14-0 ]
YieldReaction ConditionsOperation in experiment
94% With potassium phosphate; (NC5H3(N2C7H4(CH2)3CH3)2)NiBr(1+)*Br(1-)=Ni(NC5H3(N2C7H4(CH2)3CH3)2)Br2; triphenylphosphine; In 1,4-dioxane; at 80℃; for 24h;Schlenk technique; General procedure: To a 50mL Schlenk tube containing benzylic ammonium iodide (0.5mmol), arylboronic acid (2.0mmol), K3PO4 (2.25mmol), castalyst (5molpercent) and PPh3 (20molpercent) were added and the tube was purged with N2 for 3 times. Then 1,4-dioxane (2.0mL), subsequently, was introduced to the tube. The resulted mixture was allowed to stir for 24h at 80°C under atmosphere of N2. After the completion of the reaction, the resulting mixture was filtered through a Celite pad and concentrated under the vacuum and directly purified by flash chromatography to give the desired product.
82% With potassium phosphate; palladium diacetate; XPhos; In tetrahydrofuran; at 50℃; for 14h;Sealed tube; Inert atmosphere; General procedure: The desired amount of substrate, boronic acid (3 equiv), base (3equiv), Pd(OAc)2 (2.5 molpercent) and ligand (5 molpercent) were weighed out as solids, the vial was sealed and purged with argon, then solvent was added and the vial was purged again. The reactions were run for 14 h at the specified temperature. The crude material was filtered through a pad of Celite and washed three times with CHCl3. The solvent was removed under reduced pressure, an internal standard was added and the reaction was analysed by 1H NMR spectroscopy. For purification, the analysed mixture was concentrated, the product extracted with Et2O and filtered through anhydrous MgSO4 and further purified by flash column chromatography.
 

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