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Chemical Structure| 1000519-40-3 Chemical Structure| 1000519-40-3

Structure of 1000519-40-3

Chemical Structure| 1000519-40-3

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Product Details of [ 1000519-40-3 ]

CAS No. :1000519-40-3
Formula : C10H11F3O2
M.W : 220.19
SMILES Code : OCCCC1=CC=C(OC(F)(F)F)C=C1
English Name :3-(4-(Trifluoromethoxy)phenyl)propan-1-ol
MDL No. :MFCD09927393

Safety of [ 1000519-40-3 ]

Application In Synthesis of [ 1000519-40-3 ]

* 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 [ 1000519-40-3 ]

[ 1000519-40-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 886499-74-7 ]
  • [ 1000519-40-3 ]
YieldReaction ConditionsOperation in experiment
With dimethylsulfide borane complex In tetrahydrofuran at 0 - 20℃; for 18h; General procedure for obtaining derivatives of (3-Bromopropyl)benzene General procedure: To a stirred solution of 3- or 4-substituted phenylpropanoic acid 51-63 (7.0 mmol) in dry THF (35 ml), borane dimethyl sulfide (21.0 mmol) was added dropwise at 0 oC. The reaction mixture was stirred for 18h at room temperature, quenched with H2O and concentrated in vacuo. The resulting residue was re-dissolved in diethyl ether (25 ml), and washed with 10%NaOH (30ml) and brine. The organic fraction was dried over Na2SO4, filtered, and concentrated in vacuo to give 3-phenylpropan-1-ol derivatives that were used in the next step without further purification.
100 % Stage #1: 3-(4-(trifluoromethoxy)phenyl)propanoic acid With sodium tetrahydroborate In tetrahydrofuran at 0℃; Stage #2: With boron trifluoride diethyl etherate In tetrahydrofuran at 0 - 20℃; 227 Synthesis of Intermediate III-47 Add 4-trifluoromethoxyphenylpropionic acid (400 mg, 1.71 mmol) to anhydrous tetrahydrofuran (4 mL), add sodium borohydride (130 mg, 3.41 mmol) in batches under ice bath, continue stirring at 0°C for 10 minutes, and observe After the bubbles stop generating, add boron trifluoride ether (222 μL, 1.80 mmol) dropwise. After the drops are completed, slowly rise to room temperature and react for 8 hours. After the reaction, add water (20 mL) to the reaction solution to quench, extract with ethyl acetate (10 mL x 3), combine the organic phases, wash with saturated brine (10 mL x 1), dry over anhydrous sodium sulfate, filter, and evaporate the solvent under reduced pressure. , to obtain intermediate III-47 (light yellow oily liquid, 379 mg).
100 % Stage #1: 3-(4-(trifluoromethoxy)phenyl)propanoic acid With sodium tetrahydroborate In tetrahydrofuran at 0℃; Stage #2: With boron trifluoride diethyl etherate In tetrahydrofuran at 0 - 20℃; 227 Synthesis of Intermediate III-47 Add 4-trifluoromethoxyphenylpropionic acid (400 mg, 1.71 mmol) to anhydrous tetrahydrofuran (4 mL), add sodium borohydride (130 mg, 3.41 mmol) in batches under ice bath, continue stirring at 0°C for 10 minutes, and observe After the bubbles stop generating, add boron trifluoride ether (222 μL, 1.80 mmol) dropwise. After the drops are completed, slowly rise to room temperature and react for 8 hours. After the reaction, add water (20 mL) to the reaction solution to quench, extract with ethyl acetate (10 mL x 3), combine the organic phases, wash with saturated brine (10 mL x 1), dry over anhydrous sodium sulfate, filter, and evaporate the solvent under reduced pressure. , to obtain intermediate III-47 (light yellow oily liquid, 379 mg).
 

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