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Chemical Structure| 147219-20-3 Chemical Structure| 147219-20-3

Structure of 147219-20-3

Chemical Structure| 147219-20-3

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Product Details of [ 147219-20-3 ]

CAS No. :147219-20-3
Formula : C11H12O2
M.W : 176.21
SMILES Code : O=C(O)/C=C/C1=CC=C(C)C(C)=C1
MDL No. :MFCD00017541

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Application In Synthesis of [ 147219-20-3 ]

* 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 [ 147219-20-3 ]

[ 147219-20-3 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 147219-20-3 ]
  • [ 25173-76-6 ]
YieldReaction ConditionsOperation in experiment
98% With hydrogen In methanol at 20℃; for 4 h; A mixture of 3-(3,4-dimethyl-phenyl)-acrylic acid (19.269 g; 109.355 mmol) and 10percent palladium over activated charcoal (1.920 g) was placed under nitrogen before methanol (300 ml) was carefully added. The resulting suspension was placed under vacuum, then under hydrogen (1 atm), and the reaction mixture was vigorously stirred at rt for 4h. The reaction mixture was filtered over a pad of celite, and concentrated under reduced pressure to give the expected product 3- (3,4-dimethyl-phenyl)-propionic acid as a grey solid which was further dried under HV (19.070 g; 98percent). LC-MS: tR = 0.85 min; [M+H]+: no ionisation.
98% With hydrogen In methanol at 20℃; for 4 h; A mixture of 3-(3,4-dimethyl-phenyl)-acrylic acid (19.269 g; 109.355 mmol) and 10percent palladium over activated charcoal (1.920 g) was placed under nitrogen before MeOH (300 ml) was carefully added. The resulting suspension was placed under vacuum, then under hydrogen (1 atm), and the reaction mixture was vigorously stirred at rt for 4h. The reaction mixture was filtered over a pad of celite, and concentrated under reduced pressure to give the expected product 3-(3,4-dimethyl-phenyl)-propionic acid as a grey solid which was further dried under HV (19.070 g; 98percent). LC-MS: tR = 0.85 min; [M+H]+: no ionisation.
References: [1] Journal of Heterocyclic Chemistry, 1987, vol. 24, # 3, p. 677 - 682.
[2] Monatshefte fur Chemie, 1996, vol. 127, # 2, p. 185 - 200.
[3] Patent: WO2008/26149, 2008, A1, . Location in patent: Page/Page column 22.
[4] Patent: WO2008/78291, 2008, A1, . Location in patent: Page/Page column 39.
[5] Collection of Czechoslovak Chemical Communications, 1967, vol. 32, p. 4082 - 4098.
 

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