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Chemical Structure| 6372-02-7 Chemical Structure| 6372-02-7

Structure of 6372-02-7

Chemical Structure| 6372-02-7

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Product Details of [ 6372-02-7 ]

CAS No. :6372-02-7
Formula : C3H3IO2
M.W : 197.96
SMILES Code : O=C(/C=C/I)O
MDL No. :MFCD09265244

Safety of [ 6372-02-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 6372-02-7 ]

* 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 [ 6372-02-7 ]

[ 6372-02-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 6214-35-3 ]
  • [ 6372-02-7 ]
YieldReaction ConditionsOperation in experiment
95% With hydrogen iodide; In water; benzene; at 80℃; for 5h; To a solution of 55% aqueous HI (0.3 mL) and benzene(4.3 mL) was added (Z)- propenoic acid (3.6 g, 18 mmol). The mixture was heated at80 C for 5 h. After the mixture cooled to room temperature, ether was added, and thelayers were separated. The aqueous layer was extracted with ether, and the combinedorganic layers were washed with aqueous Na2S2O3 and dried (MgSO4). The solventwas evaporated in vacuo. The residue was washed with n-hexane, giving 3.4 g of(E)-propenoic acid in 95% yield as a white crystal. The spectral data was inaccordance with the literature [1].
89% With hydrogen iodide; In water; benzene; at 80℃; for 5h; The procedure of Step 2 was carried out according to the protocol put forth by Takeuchi et al, Journal of Organic Chemistry, 2000 (65), 1558-61. (Z)-3- Iodo-acrylic acid (5.94 g, 30 mmol)was added to a solution of 55% aqueous hydroiodic acid (0.6 mL) and benzene (8 mL). The mixture was heated at 800C for 5 hours, cooled to ambient temperature, diluted with ether and extracted. The aqueous layer was extracted with ether, and the combined organic layers were washed with aqueous sodium thiosulphate and dried magnesium sulfate. The solvent was evaporated in vacuo. The solvent was evaporated in vacuo, <n="63"/>and the residue was washed with n-hexane to give the title compound as a pale yellow solid, yield 5.29 g (89%); mp 144-147 0C. 1H NMR (270 MHz, CDCl3) δ 6.90 (d, J = 14.8 Hz, IH), 8.09 (d, J = 14.8 Hz, IH), 10.0 (br, IH). 13C NMR (67.8 MHz, CDCl3) δ 103.2, 135.7, 169.4.
  • 2
  • [ 471-25-0 ]
  • [ 6214-35-3 ]
  • [ 6372-02-7 ]
  • 3
  • [ 471-25-0 ]
  • [ 6214-35-3 ]
  • [ 6372-02-7 ]
  • [ 927867-71-8 ]
  • 4
  • [ 6372-02-7 ]
  • [ 6214-35-3 ]
 

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