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Chemical Structure| 83612-52-6 Chemical Structure| 83612-52-6

Structure of 83612-52-6

Chemical Structure| 83612-52-6

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Product Details of [ 83612-52-6 ]

CAS No. :83612-52-6
Formula : C10H9ClO
M.W : 180.63
SMILES Code : O=C(Cl)/C=C/C1=CC=CC=C1C
MDL No. :MFCD03424736

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Application In Synthesis of [ 83612-52-6 ]

* 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 [ 83612-52-6 ]

[ 83612-52-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 939-57-1 ]
  • [ 83612-52-6 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In toluene; for 4h;Reflux; In a 250 ml round bottom flask there were placed: 5 g frans-2-methylcinnamic acid, 30 ml toluene and 5 ml thionyl chloride (d=1.63 g/ml). The reaction mixture was refluxed for 4 hours, then solvents were evaporated under reduced pressure, 10 ml of toluene was added twice and evaporated.
With thionyl chloride; In toluene; for 5h;Reflux; General procedure: Syntheses of the tested compounds were carried out according to Scheme 1. The compounds were obtained by means of N-acylation of aminoalkanols by means of substituted cinnamic acid chlorides.20-22 4-Chloro, 4-methyl, and 2-methylcinnamic acid chlorides were obtained in the reactions of 4-chloro, 4-methyl, and 2-methylcinnamic acid with 10% excess of thionyl chloride in toluene. The reagents were refluxed for 5 h, then the solvent was evaporated under reduced pressure. In case of 4-Cl and 4-CH3-cinnamic acid chlorides the oily residues were crystallized from n-hexane what resulted in obtaining yellowish-white products, while 2-CH3-cinnamic acid chloride was not obtained in crystalline form and was used as a brown liquid.
With thionyl chloride; In 1,2-dichloro-ethane; N,N-dimethyl-formamide;Reflux; 2-methylcinnamic acid (II-2,5 mmol) was dissolved in dichloroethane (10 mL), thionyl chloride (15 mmol) and DMF (1 drop). The mixture was heated to reflux for overnight. The next day, the reaction mixture was concentrated to dryness under reduced pressure to give cinnamoyl chloride (III-2) as an oily intermediate.
 

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