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Chemical Structure| 93983-13-2 Chemical Structure| 93983-13-2

Structure of 93983-13-2

Chemical Structure| 93983-13-2

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Product Details of [ 93983-13-2 ]

CAS No. :93983-13-2
Formula : C9H11ClO3
M.W : 202.63
SMILES Code : OCC1=CC=C(OC)C(OC)=C1Cl
MDL No. :MFCD00210141
InChI Key :ZXYBQLFOEYWYBM-UHFFFAOYSA-N
Pubchem ID :2775134

Safety of [ 93983-13-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 93983-13-2 ]

* 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 [ 93983-13-2 ]

[ 93983-13-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5417-17-4 ]
  • [ 93983-13-2 ]
YieldReaction ConditionsOperation in experiment
With sodium tetrahydroborate; In ethanol; at 20℃; <strong>[5417-17-4]2-Chloro-3,4-dimethoxybenzaldehyde</strong> (2.5 g, 12.4 mmol) was dissolved in ethanol (50 ml), sodium borohydride (930 mg, 25 mmol) was added, and the mixture was stirred overnight at room temperature. A treatment according to a conventional method using ethyl acetate as an extraction solvent gave a crude product. The obtained crude product was dissolved in thionyl chloride (5 ml) and, after stirring at room temperature for 4 hr, treated according to a conventional method using ethyl acetate as an extraction solvent. The obtained crude product was dissolved in dimethyl sulfoxide (30 ml), sodium cyanide (610 mg, 12.4 mmol) was added, and the mixture was stirred overnight at room temperature. A treatment according to a conventional method using ethyl acetate as an extraction solvent gave a crude product, which was successively purified by silica gel column chromatography to give a nitrile intermediate (830 mg, 3.93 mmol)
With sodium tetrahydroborate; In dichloromethane; at 20℃; for 0.5h; General procedure: To a solution of various benzaldehydes 4aew (10 mmol) dissolved in methanol (50 mL) was added sodium borohydride (20 mmol) at room temperature, and the mixturewas stirred at the same temperature for 30 min and concentrated under reduced pressure. The residue was diluted with methylene chloride (500 mL) and washed with water, and dried over anhydrous Na2SO4, and concentrated under reduced pressure to give the corresponding crude phenylmethanols 5a-w
 

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