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Chemical Structure| 1514304-24-5 Chemical Structure| 1514304-24-5

Structure of 1514304-24-5

Chemical Structure| 1514304-24-5

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Product Details of [ 1514304-24-5 ]

CAS No. :1514304-24-5
Formula : C7H5BrClFO
M.W : 239.47
SMILES Code : OCC1=CC(Br)=CC(Cl)=C1F
MDL No. :MFCD29036608
Boiling Point : No data available

Safety of [ 1514304-24-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362

Application In Synthesis of [ 1514304-24-5 ]

* 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 [ 1514304-24-5 ]

[ 1514304-24-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1280786-80-2 ]
  • [ 1514304-24-5 ]
YieldReaction ConditionsOperation in experiment
96.6% With methanol; sodium tetrahydroborate; at 20℃; for 2h; To a solution of <strong>[1280786-80-2]5-bromo-3-chloro-2-fluorobenzaldehyde</strong> (4.7 g, 19.9 mmol, 1.0 eq.) in CH3OH (30 mL) was added NaBH4 (2.3 g, 59.7 mmol, 3.Oeq,) in portions. The mixture was stirred at r.t. for 2 h until TLC showed that the reaction was completed, then concentrated under reduced pressure. The residue was dissolved in EA (60 mL), washed with brine (60 mLx3), dried over anhydrous Na2SO4 and concentrated to provide (5-bromo-3- chloro-2-fluorophenyl)methanol (4.6 g, 96.6%).
96.6% With methanol; sodium tetrahydroborate; at 20℃; for 2h; To a solution of <strong>[1280786-80-2]5-bromo-3-chloro-2-fluorobenzaldehyde</strong> (4.7 g, 19.9 mmol, 1.0 eq.) in CH3OH (30 mL) was added NaBH4 (2.3 g, 59.7 mmol, 3.0eq,) in portions. The mixture was stirred at r.t. for 2 h until TLC showed that the reaction was completed, then concentrated under reduced pressure. The residue was dissolved in EA (60 mL), washed with brine (60 mLx3), dried over anhydrous Na2S04 and concentrated to provide (5-bromo-3-chloro-2-fluorophenyl)methanol (4.6 g, 96.6%).
55% With sodium tetrahydroborate; In tetrahydrofuran; for 1h;Cooling with ice; To an ice-water cooled solution of compound S2 (18.0 g, 0.076 mol) in THF (150 mL) was added NaBH4(4.3 g, 0.114 mol). The reaction mixture was stirred at this temperature for 1 h. Then the reaction mixture was quenched slowly with aq. NH4Cl and extracted with ethyl acetate (500 mL). The organic phase was washed with brine, dried over anhydrous Na2SO4, filtered, and then concentrated. The residue was purified by column chromatography on silica gel (eluted with petroleum ether/ethyl acetate=100:1 to 20:1) to give compound S3 (10 g, yield 55%) as a white solid.
 

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