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Chemical Structure| 53392-07-7 Chemical Structure| 53392-07-7

Structure of 53392-07-7

Chemical Structure| 53392-07-7

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Product Details of [ 53392-07-7 ]

CAS No. :53392-07-7
Formula : C11H16O
M.W : 164.24
SMILES Code : OCCCCC1=CC=C(C)C=C1
MDL No. :MFCD11592101

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* 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 [ 53392-07-7 ]

[ 53392-07-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4521-22-6 ]
  • [ 53392-07-7 ]
YieldReaction ConditionsOperation in experiment
Synthesis of 4-(4-Methylphenyl) butanol To lithium aluminum hydride (427 mg, 11.2 mmol) suspended in dry ether (5 ml) at 0 C. is added 1 g of 4-(4-methylphenyl) butanoic acid (5.614 mmol) dissolved in dry ether (10 ml) over a period of 30 minutes. The reaction mixture is then warmed to room temperature and stirred for 4 hours. Water (0.43 ml), NaOH (15% solution, 0.43 g) and water (1.29 ml) are then added successively and the resulting solution is stirred for 30 minutes. The precipitate is filtered and washed with ether and dried. This is then concentrated and purified by flash chromatography (silica gel; ethyl acetate/hexanes) as the eluding medium.
Synthesis of 4-(4-Methylphenyl) butanol To lithium aluminum hydride (427 mg, 11.2 mmol) suspended in dry ether (5 ml) at 0 C. is added 1 g of 4-(4-methylphenyl) butanoic acid (5.614 mmol) dissolved in dry ether (10 ml) over a period of 30 minutes. The reaction mixture is then allowed to warm to room temperature and stirred for 4 hours. Water (0.43 ml), NaOH (15% solution, 0.43 g) and water (1.29 ml) were then added successively and the resulting solution is stirred for 30 minutes. The resulting precipitate is filtered and washed with ether and dried.
With lithium aluminium tetrahydride; In diethyl ether; at 20℃; for 4h; To lithium aluminum hydride (427 mg, 11.2 mmol) suspended in dry ether (5 ml) at 0 C. is added 1 g of 4-(4- methylphenyl)butanoic acid (5.614 mmol) dissolved in dry ether (10 ml) over a period of 30 minutes. The reaction mixture is then allowed to warm to room temperature and stirred for 4 hours. Water (0.43 ml), NaOH (15% solution, 0.43 g)and water (1.29 ml) were then added successively and theresulting solution is stirred for 30 minutes. The resultingprecipitate is filtered and washed with ether and dried. The filtrate is then concentrated and purified by flash chromatography using ethyl acetate-hexanes as the eluting medium.
 

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