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Chemical Structure| 53391-61-0 Chemical Structure| 53391-61-0

Structure of 53391-61-0

Chemical Structure| 53391-61-0

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Product Details of [ 53391-61-0 ]

CAS No. :53391-61-0
Formula : C5H7NS
M.W : 113.18
SMILES Code : CSC1=CC=CN1
MDL No. :MFCD09952556

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Application In Synthesis of [ 53391-61-0 ]

* 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 [ 53391-61-0 ]

[ 53391-61-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 53391-61-0 ]
  • [ 24167-56-4 ]
  • [ 80965-01-1 ]
  • 2
  • [ 53391-61-0 ]
  • ethyl acetate n-hexane [ No CAS ]
  • [ 24167-56-4 ]
  • [ 80965-01-1 ]
YieldReaction ConditionsOperation in experiment
54% With sodium acetate; trichlorophosphate; In water; 1,2-dichloro-ethane; EXAMPLE 10 Preparation of 2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (Step 2) A solution of <strong>[24167-56-4]N,N-dimethyl-4-fluorobenzamide</strong> (8.4 g, 0.05 moles) in anhydrous 1,2-dichloroethane (170 ml) containing phosphorous oxychloride (7.7 g, 0.05 moles) was heated at reflux temperature for 1 hour. At the end of this time 2-methylthiopyrrole (2.82 g, 0.025 moles) was added and heating was continued for an additional 0.5 hour. The solution was cooled to room temperature, and to the cooled solution was cautiously added, with good agitation, a solution of sodium acetate (12.3 g, 0.15 moles) in water (50 ml) and the mixture was then boiled under reflux for 1 hour. The organic phase was separated, washed with water, dried, and evaporated. The residue was subjected to column chromatography on silica gel using ethyl acetate-hexane (1:9) as the eluding solvent. A yellow colored solid 2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (3.2 g, 54%) was obtained which after crystallization from ether-hexane had m.p. 112-113 C. UV: (MeOH) 218.5, 248, 343 nm(epsilon9770, 8510, 13,800). IR: (CHCl3) 3440, 3250, 1610 cm-1.
54% With sodium acetate; trichlorophosphate; In water; 1,2-dichloro-ethane; EXAMPLE 10 Preparation of 2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (Step 2) A solution of <strong>[24167-56-4]N,N-dimethyl-4-fluorobenzamide</strong> (8.4 g, 0.05 moles) in anhydrous 1,2-dichloroethane (170 ml) containing phosphorus oxychloride (7.7 g, 0.05 moles) was heated at reflux temperature for 1 hour. At the end of this time 2-methylthiopyrrole (2.82 g, 0.025 moles) was added and heating was continued for an additional 0.5 hour. The solution was cooled to room temperature, and to the cooled solution was cautiously added, with good agitation, a solution of sodium acetate (12.3 g, 0.15 moles) in water (50 ml) and the mixture was then boiled under reflux for 1 hour. The organic phase was separated, washed with water, dried, and evaporated. The residue was subjected to column chromatography on silica gel suing ethyl acetate-hexane (1:9) as the eluding solvent. A yellow colored solid 2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (3.2 g, 54%) was obtained which after crystallization from ether-hexane had m.p. 112-113 C. UV: (MeOH) 218.5, 248, 343 nm (epsilon 9770, 8510, 13,800). IR: (CHCl3) 3440, 3250, 1610 cm-1. NMR: (CDCl3) 2.48 (s, 3H); 6.25 (q, 1H; J=2.5, 4 Hz); 6.80 (q, 1H; J=2.5, 4 Hz); 7.12 (q, 2H; J=8, 8); 7.92 (q, 2H; J=5.5, 8); 10.67 (s, 1H, WH=22). Calcd. for C12 H10 FNOS: C, 61.24; H, 4.28. Found: C, 61.01; H, 4.21.
 

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