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Chemical Structure| 82477-68-7 Chemical Structure| 82477-68-7

Structure of 82477-68-7

Chemical Structure| 82477-68-7

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Product Details of [ 82477-68-7 ]

CAS No. :82477-68-7
Formula : C8H9ClO2
M.W : 172.61
SMILES Code : OCC1=CC(OC)=CC(Cl)=C1
MDL No. :MFCD08234652

Safety of [ 82477-68-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 82477-68-7 ]

* 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 [ 82477-68-7 ]

[ 82477-68-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 82477-68-7 ]
  • [ 885270-32-6 ]
YieldReaction ConditionsOperation in experiment
79% With phosphorus tribromide; In diethyl ether; at 0 - 20℃; for 2h; To a solution of (3-chloro-5-methoxyphenyl)methanol (2.0 g, 1 1 .6 mmol) in diethyl ether (20 ml_) at 0 C was added phosphorus tribromide (0.5 ml_). The reaction mixture was stirred at 0 C for 2 h. Reaction was poured into saturated aqueous sodium bicarbonate (150 ml_) and extracted with ethyl acetate (200 ml_ x 2). The combined organic phases were dried over sodium sulfate, filtered and concentrated to afford 1 -(bromomethyl)-3-chloro-5-methoxybenzene (2.15 g, 9.16 mmol, 79%) as a light-yellow solid. Used in the next step directly without additional purification.
With phosphorus tribromide; In diethyl ether; at 0℃; for 0.5h; (iii) (3-chIoro-5-methoxyphenyl)acetonitrilePhosphorous tribromide (0.28 ml) was added to a solution of the product of step (ii) (1.55 g) in ether (20 ml) at 0 0C, then stirred for 30 min. The reaction mixture was partitioned between ether and aqueous sodium hydrogen carbonate, the organics were separated then dried (MgSO4) and evaporated under reduced pressure. The residue was dissolved in DMF (20 ml) and sodium cyanide (0.5 g) was added. The mixture was stirred overnight then partitioned between ether and water; the organics were separated, washed with aqueous sodium hydrogen carbonate then dried (MgSO4) and evaporated under reduced pressure. The residue was purified by flash column chromatography (eluent 1:1 ether/ isohexane) to give the subtitle compound (0.53g).1H NMR CDCl3-d6: delta 6.91-6.9 (IH, m), 6.86-6.85 (IH, m), 6.77-6.76 (IH, m), 3.79 (3H, s), 3.69 (2H, s).
With phosphorus tribromide; In diethyl ether; at 0℃; for 0.5h; Phosphorous tribromide (0.28 ml) was added to a solution of the product of step (ii) (1.55 g) in ether (20 ml) at 0 C., then stirred for 30 min. The reaction mixture was partitioned between ether and aqueous sodium hydrogen carbonate, the organics were separated then dried (MgSO4) and evaporated under reduced pressure. The residue was dissolved in DMF (20 ml) and sodium cyanide (0.5 g) was added. The mixture was stirred overnight then partitioned between ether and water; the organics were separated, washed with aqueous sodium hydrogen carbonate then dried (MgSO4) and evaporated under reduced pressure. The residue was purified by flash column chromatography (eluent 1:1 ether/isohexane) to give the subtitle compound (0.53 g). 1H NMR CDCl3-d6: delta 6.91-6.9 (1H, m), 6.86-6.85 (1H, m), 6.77-6.76 (1H, m), 3.79 (3H, s), 3.69 (2H, s).
 

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