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Chemical Structure| 1355488-96-8 Chemical Structure| 1355488-96-8

Structure of 1355488-96-8

Chemical Structure| 1355488-96-8

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Product Details of [ 1355488-96-8 ]

CAS No. :1355488-96-8
Formula : C10H10F2O2
M.W : 200.18
SMILES Code : O=C(OCC)C1=CC(F)=C(C)C=C1F

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Application In Synthesis of [ 1355488-96-8 ]

* 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 [ 1355488-96-8 ]

[ 1355488-96-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 103877-80-1 ]
  • [ 64-17-5 ]
  • [ 1355488-96-8 ]
YieldReaction ConditionsOperation in experiment
95% With sulfuric acid; for 18h;Reflux; Preparation 18Ethyl 2 ,5-difl uoro-4-meth yl benzoateTo a solution of <strong>[103877-80-1]2,5-difluoro-4-methylbenzoic acid</strong> (5 g, 2.904 mmol) in ethanol (100 ml_) was added concentrated sulfuric acid (1 ml_). The reaction mixture was stirred at reflux for 18 hours. LCMS showed complete consumption of starting material, so the solvents were removed in vacuo and the resulting residue redissolved in EtOAc (50 ml_), and washed with saturated aqueous sodium bicarbonate. The organic layer was separated, and the aqueous layer extracted with EtOAc (2 x 50 ml_). The combined organics were dried over sodium sulfate and evaporated to yield the title compound as a pale yellow oil (5.502 g, 95%).1H NMR (CDCIs, 400 MHz): delta 1 .38 (t, 3H), 2.30 (d, 3H), 4.37 (q, 2H), 6.95 (dd, 1 H), 7.55 (dd, 1 H).LCMS Rt = 3.06 minutes. MS m/z molecular ion not observed.
With thionyl chloride; at 70℃; for 18h; To a solution of <strong>[103877-80-1]2,5-difluoro-4-methylbenzoic acid</strong> (595 mg, 3.89 mmol) in ethanol (30 ml_) was added a catalytic amount of thionyl chloride (2 drops). The reaction was stirred for 18 hours at 70 C, and cooled to room temperature. The solvent was removed in vacuo to afford the title compound as a clear oil (500 mg, 86%). No further purification undertaken. 1H NMR (400 MHz, CDCI3): delta 1 .30 (t, 3H), 2.30 (s, 3H), 4.40 (q, 2H), 6.90 (m, 1 H), 7.60 (m, 1 H). LCMS Rt = 3.53 minutes MS no mass ion observed.
 

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