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5-Chloro-N-tert-butyl-2-thiophenesulfonamide

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5-Chloro-N-tert-butyl-2-thiophenesulfonamide Basic information

Product Name:
5-Chloro-N-tert-butyl-2-thiophenesulfonamide
Synonyms:
  • N-tert-Butyl-5-chlorothiophene sulfonamide
  • 5-Chlorothiophene-2-sulfonic acid tert-butylamide
  • 5-Chloro-N-tert-butyl-2-thiophenesulfonamide
  • N-(tert-Butyl)-5-chlorothiophene-2-sulfonamide
  • N-(tert-Butyl)-5-chlorothiophene-2-sulphonamide
  • N-tert-Butyl 5-Chloro-2-thiophenesulfonamide
  • 2-Thiophenesulfonamide, 5-chloro-N-(1,1-dimethylethyl)-
  • 5-Chloro-N-tert-butyl-2-thiophenesulfonamide ISO 9001:2015 REACH
CAS:
155731-14-9
MF:
C8H12ClNO2S2
MW:
253.77
Product Categories:
  • Thiophene intermediates
  • API intermediates
Mol File:
155731-14-9.mol
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5-Chloro-N-tert-butyl-2-thiophenesulfonamide Chemical Properties

Boiling point:
349.1±52.0 °C(Predicted)
Density 
1.328
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
11.53±0.50(Predicted)
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Safety Information

Hazard Codes 
Xi
HS Code 
2934999090
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5-Chloro-N-tert-butyl-2-thiophenesulfonamide Usage And Synthesis

Synthesis

2766-74-7

75-64-9

155731-14-9

A. General procedure for the synthesis of (tert-butyl)[(5-chloro(2-thienyl))sulfonyl]amine (0316): 5.5 g (27.5 mmol) of 5-chlorothiophene-2-sulfonyl chloride was dissolved in anhydrous THF at 0 °C, and 5.7 mL (75.5 mmol) of tert-butyl amine was slowly added. The reaction mixture was gradually warmed to 23 °C and the reaction was stirred. After completion of the reaction, the reaction mixture was diluted with 125 mL of ether and filtered to remove insoluble material. The filtrate was washed sequentially with 1N HCl and brine and then dried over anhydrous MgSO4. Finally, the solvent was removed by vacuum concentration to give 6.4 g (98% yield) of the target compound as an oil.

References

[1] Patent: EP2314593, 2016, B1. Location in patent: Paragraph 0316
[2] Pharmazie, 1994, vol. 49, # 2-3, p. 115 - 117
[3] Patent: US2002/77486, 2002, A1
[4] Patent: US6906063, 2005, B2

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