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Chemical Structure| 51934-45-3 Chemical Structure| 51934-45-3

Structure of 51934-45-3

Chemical Structure| 51934-45-3

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Product Details of [ 51934-45-3 ]

CAS No. :51934-45-3
Formula : C14H14O2
M.W : 214.26
SMILES Code : O=C(OCC)C1=C2C=CC=CC2=C(C)C=C1

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Application In Synthesis of [ 51934-45-3 ]

* 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.

  • Downstream synthetic route of [ 51934-45-3 ]

[ 51934-45-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64-17-5 ]
  • [ 4488-40-8 ]
  • [ 51934-45-3 ]
YieldReaction ConditionsOperation in experiment
94% With sulfuric acid; for 16h;Reflux; In a two necked flask, 186 mg of 4-methyl-1-naphthoic acid (1.00 mmol, 1.0 eq) was dissolved in 5 mL of ethanol and was stirred under reflux. Then 5-6 drops of sulfuric acid was added into mixture. After 16 hours, the solution was cooled down to room temperature and extracted with ethyl acetate (3x25 mL). The combined organic phase was dried over anhydrous MgSO4. Then, the organic layer was filtered and concentrated under reduced pressure to yield crude product. Purification of the crude product by silica gel column chromatography (EtOAc/Hex; 1:10) resulted 201 mg of desired product in 94% yield. Rf: 0.50 (1:8 EtOAc-Hex)1H-NMR (400 MHz, CDCl3) delta 9.03 (d, J = 8.6 Hz, 1H), 8.11 (d, J = 7.4 Hz, 1H), 8.05 (d, J = 8.2 Hz, 1H), 7.67 - 7.54 (m, 2H), 7.34 (d, J = 7.4 Hz, 1H), 4.49 (q, J = 7.2 Hz, 2H), 2.73 (s, 3H), 1.48 (t, J = 7.0 Hz, 3H)13C-NMR (100 MHz, CDCl3) delta 167.88, 140.25, 133.01, 131.55, 130.05, 127.38, 126.51, 126.13, 125.99, 125.65, 124.55, 61.04, 20.27, 14.57.HRMS [M+H]+ (C14H15O2) Calculated: 215.1072; Found: 215.1084
87% With thionyl chloride; for 6h;Reflux; To a solution of 20-1 (5 g, 26.9 mmol) in ethanol (50 mL) was added thionyl chloride (4.8 g, 40.32 mmol) at 0 C and stirred at reflux for 6 hr. The reaction mixture was distilled off and diluted with EtOAc (100 mL), washed with water (100 mL), NaHC03 solution (50 mL) and dried over Na2S04, and concentrated under reduced pressure. The crude compound was purified using silica gel chromatography (10% EtOAc in hexanes) to afford 20-2 (5 g, 23.63 mmol, 87% yield) as a brown oily liquid. MS (ESI): m/z 215.1 (M+l)+.
 

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