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Chemical Structure| 1016646-16-4 Chemical Structure| 1016646-16-4

Structure of 1016646-16-4

Chemical Structure| 1016646-16-4

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Product Details of [ 1016646-16-4 ]

CAS No. :1016646-16-4
Formula : C8H8ClFO
M.W : 174.60
SMILES Code : C[C@H](C1=CC=C(Cl)C=C1F)O

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Application In Synthesis of [ 1016646-16-4 ]

* 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 [ 1016646-16-4 ]

[ 1016646-16-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 175711-83-8 ]
  • [ 1016646-16-4 ]
YieldReaction ConditionsOperation in experiment
With (+)-B-chlorodiisopinocamphenylborane; In tetrahydrofuran; hexane; at -78 - -25℃; for 7h;Inert atmosphere; 107621 To a solution of <strong>[175711-83-8]1-(4-chloro-2-fluorophenyl)ethan-1-one</strong> (10 g, 58 mmol) in tetrahydrofuran (100 mL) at -78 C under a nitrogen atmosphere was added (+)-B20 Chlorodiisopinocampheylborane (50 to 60% wt in hexanes, 9.2 mL, 64 mmol), slowly. The resultingmixture was slowly warmed to -25 C and stirred at this temperature for 2 h. 1-(4-Chloro-2- fluorophenyl)ethan-1-one was detected by LCMS (?liquid chromatography mass spectrometry?) and HPLC, and the mixture was cooled back to -78 C. Additional (+)-BChlorodiisopinocampheylborane (50 to 65% wt in hexanes, 5.4 mL, 38 mmol) was added to themixture at -78 C. The resulting mixture was slowly warmed to -25 C and stirred at this temperature for 5 h. Diethanolamine (18 mL, 191 mmol) was added to the reaction mixture, which was then stirred at room temperature for 3 d. The reaction was filtered, and the filtrate was concentrated and purified by silica gel chromatography (0 to 30% ethyl acetate in hexanes) to afford 18.8 g impure (R)- 1 -(chloro-2-fluorophenyl)ethan- 1 -ol.
18.8 g To a solution of <strong>[175711-83-8]1-(4-chloro-2-fluorophenyl)ethan-1-one</strong> (10 g, 58 mmol) in THF (100 mL) at -78 C. under a nitrogen atmosphere was added (+)-DIP-Cl (50 to 60% wt in hexanes, 9.2 mL, 64 mmol), slowly. The resulting mixture was slowly warmed to -25 C. and stirred at this temperature for 2 h. 1-(4-Chloro-2-fluorophenyl)ethan-1-one was detected by LCMS and HPLC, and the mixture was cooled back to -78 C. Additional (+)-DIP-Cl (50 to 65% wt in hexanes, 5.4 mL, 38 mmol) was added to the mixture at -78 C. The resulting mixture was slowly warmed to -25 C. and stirred at this temperature for 5 h. Diethanolamine (18 mL, 191 mmol) was added to the reaction mixture, which was then stirred at room temperature for 3 d. The reaction was filtered, and the filtrate was concentrated and purified by silica gel chromatography (0 to 30% ethyl acetate in hexanes) to afford 18.8 g impure (R)-1-(chloro-2-fluorophenyl)ethan-1-ol.
 

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