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Chemical Structure| 13191-29-2 Chemical Structure| 13191-29-2

Structure of 13191-29-2

Chemical Structure| 13191-29-2

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Product Details of [ 13191-29-2 ]

CAS No. :13191-29-2
Formula : C7H6OS
M.W : 138.19
SMILES Code : C=CC(C1=CC=CS1)=O

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Application In Synthesis of [ 13191-29-2 ]

* 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 [ 13191-29-2 ]

[ 13191-29-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5424-47-5 ]
  • [ 13191-29-2 ]
  • 2
  • [ 13191-29-2 ]
  • [ 5650-52-2 ]
YieldReaction ConditionsOperation in experiment
28% With sulfuric acid; In 1,2-dichloro-ethane; at 20 - 80℃; for 1.25h; To a solution of 1-(thiophen-2-yl)-prop-2-en-1-one (8.5 g; 62 mmoles) of Example 1b in 1,2-dichloroehane (47 mL) a solution of sulphuric acid (47 mL) is added dropwise at room temperature. The mixture is then heated to 80C for 75 minutes. Then cooling to room temperature is carried out and the cooled liquid mass is poured in an ice bath. An extraction with dichloromethane (2 x 20 mL) is then carried out and the organic phase washed with a 5% NaHCO3 solution, anhydrified with sodium sulphate, filtered and concentrated under vacuum. The obtained residue is purified by chromatography on silica gel with a ligroin/ethyl acetate mixture (elution gradient from 10% to 80% ethyl acetate). After solvent removal 2.4 g of 4H-cyclopenta[b]thiophen-6(5H)-one are isolated (yellow solid; yield 28%). Rf=0.54 (ligroin/ethyl acetate 9/7 volume/volume); 1H NMR (CDCl3) delta (ppm): 7.89 (d, 1H, ArH), 7.05 (d, 1H, ArH), 3.01 (m, 4H, CH2); 13C NMR (CDCl3) delta (ppm): 197.3, 169.0, 141.2, 140.5, 124.0, 41.2, 24.0 FT-IR (film) numax: 3063.8, 1668.5, 1419.1, 1248.1, 960.7, 749.8 cm-1.
28% With sulfuric acid; In 1,2-dichloro-ethane; at 80℃; for 1.25h; 0254] To a solution of 1-(thiophen-2-yl)-prop-2-en-1-one (8.5 g; 62 mmoles) of Example 1b in 1,2-dichloroethane (47 mL) a solution of sulphuric acid (47 mL) is added dropwise at room temperature. The mixture is then heated to 80 C. for 75 minutes. Then cooling to room temperature is carried out and the cooled liquid mass is poured in an ice bath. An extraction with dichloromethane (2×20 mL) is then carried out and the organic phase washed with a 5% NaHCO3 solution, anhydrified with sodium sulphate, filtered and concentrated under vacuum. The obtained residue is purified by chromatography on silica gel with a ligroin/ethyl acetate mixture (elution gradient from 10% to 80% ethyl acetate). After solvent removal 2.4 g of 4H-cyclopenta[b]thiophen-6(5H)-one are isolated (yellow solid; yield 28%). Rf=0.54 (ligroin/ethyl acetate 9/7 volume/volume); 1H NMR (CDCl3) delta (ppm): 7.89 (d, 1H, ArH), 7.05 (d, 1H, ArH), 3.01 (m, 4H, CH2); 13C NMR (CDCl3) delta (ppm): 197.3, 169.0, 141.2, 140.5, 124.0, 41.2, 24.0 FT-IR (film) numax: 3063.8, 1668.5, 1419.1, 1248.1, 960.7, 749.8 cm-1
 

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