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Chemical Structure| 22494-48-0 Chemical Structure| 22494-48-0

Structure of 22494-48-0

Chemical Structure| 22494-48-0

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Product Details of [ 22494-48-0 ]

CAS No. :22494-48-0
Formula : C13H11ClO
M.W : 218.68
SMILES Code : OCC1=CC=C(C2=CC=C(Cl)C=C2)C=C1
MDL No. :MFCD01862510
InChI Key :SKCQMBTWYIRYCY-UHFFFAOYSA-N
Pubchem ID :12773845

Safety of [ 22494-48-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 22494-48-0 ]

* 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 [ 22494-48-0 ]

[ 22494-48-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 80565-30-6 ]
  • [ 22494-48-0 ]
YieldReaction ConditionsOperation in experiment
With sodium tetrahydroborate; In ethanol; at 50℃; for 2h; A mixture of Intermediate A1 (1.73 g, 1 equiv), sodium borohydride (0.3 g, 1 equiv) and ethanol (20 ml) was stirred until a clear solution was obtained; a gentle exotherm was observed.The temperature was raised to 50 C. and stirring continued for 2 h, then the solvent was removed in vacuo, water added to the residue, and the product extracted into dichloromethane.Drying and evaporation of the solvent gave a white solid (1.67 g).1H-NMR (CDCl3) delta 1.73 (1H,t), 4.74 (2H, d), 7.2-7.6 (8H, m),.
With sodium tetrahydroborate; ethanol; at 0 - 20℃; for 2h; To a solution of Compound IB (5.4 g, 1 mmol) in EtOH (40 mL) was added NaBH4 (0.95 g, 25 mmol) at 0 C. The mixture was stirred room temperature for 2 hours, quenched with 1 N HC1 solution (40 mL), and extracted with dichloromethane (30 mL x 3). The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and concentrated to give Compound 1C: LC-MS (ESI) m/z: 201 [M-OH]+.
 

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