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Chemical Structure| 39652-32-9 Chemical Structure| 39652-32-9

Structure of 39652-32-9

Chemical Structure| 39652-32-9

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Product Details of [ 39652-32-9 ]

CAS No. :39652-32-9
Formula : C8H9ClO
M.W : 156.61
SMILES Code : CC1=CC=C(C=C1Cl)CO
MDL No. :MFCD00016863

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Application In Synthesis of [ 39652-32-9 ]

* 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 [ 39652-32-9 ]

[ 39652-32-9 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 5162-82-3 ]
  • [ 39652-32-9 ]
YieldReaction ConditionsOperation in experiment
85% With borane-THF; In tetrahydrofuran; at 0 - 20℃; A. (3-chloro-4-methylphenyl methanol [00667] To a solution of 4-chloro-2-methylbenzoic acid (800 mg, 4.69 mmol) in THF (8 that was cooled at 0 C, BH3 THF (14 mL, 1M in THF) was added into the solution drop wise. The mixture was then stirred at r.t. overnight. Add methanol to the system at 0C slowly until no gas released. Remove the solvent and the residue was extracted with ethylacetate, concentrated the organic phase to give 894 mg of the title compound (85%). 1H NMR (400 MHz, CDC13): delta 2.36 (3H, s), 4.63 (2H, s), 7.13-7.22 (2H, m), 7.35 (1H, s).
With borane-THF; In tetrahydrofuran; at 0 - 35℃; for 16h;Inert atmosphere; To a solution of <strong>[5162-82-3]3-chloro-4-methylbenzoic acid</strong> (1.50 g) in THF (29 mL) was added dropwise borane-THF complex (1M THF solution, 17.6 mL) over 10 min under argon atmosphere at 0 C., and the reaction mixture was stirred at room temperature for 16 hr. The reaction was quenched with methanol at 0 C., and the mixture was stirred at room temperature for 1 hr. The organic solvent was evaporated under reduced pressure, and the residue was partitioned between water and ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and filtered through a pad of silica gel and NH silica gel. The filtrate was concentrated under reduced pressure to give crude (3-chloro-4-methylphenyl)methanol (1.39 g).
In the same manner as in Preparation Example 74-4, the objective compound (23.0 g) was obtained as a colorless oil from <strong>[5162-82-3]3-chloro-4-methylbenzoic acid</strong> (25.0 g). 1H-NMR(CDCl3): 2.36(3H, s), 4.65(2H, s), 7.14(1H, d, J=8 Hz), 7.23(1H, d, J=8 Hz), 7.36(1H, S)
 

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