Basic information Safety Supplier Related

3-ACETYL-1-(P-TOLYLSULFONYL)PYRROLE

Basic information Safety Supplier Related

3-ACETYL-1-(P-TOLYLSULFONYL)PYRROLE Basic information

Product Name:
3-ACETYL-1-(P-TOLYLSULFONYL)PYRROLE
Synonyms:
  • 1-TOSYL-3-ACETYLPYRROLE
  • 1-(1-Tosyl-1H-pyrrol-3-yl)ethanone
  • 1-{1-[(4-methylphenyl)sulfonyl]-1H-pyrrol-3-yl}ethanone
  • 1-(4-Tolylsulfonyl)-3-acetylpyrrole
  • 3-ACETYL-1-(P-TOLYLSULFONYL)PYRROLE
  • 3-ACETYL-1-TOSYLPYRROLE
  • 3-ACETYL-N-TOSYLPYRROLE
  • 3-acetyl-N-p-toluenesulfonylpyrrole
CAS:
106058-85-9
MF:
C13H13NO3S
MW:
263.31
Product Categories:
  • Azoles
  • blocks
Mol File:
106058-85-9.mol
More
Less

3-ACETYL-1-(P-TOLYLSULFONYL)PYRROLE Chemical Properties

Melting point:
68-72°C
Boiling point:
88 °C
Density 
1.24±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-11.38±0.70(Predicted)
Appearance
White to off-white Solid
More
Less

Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
2933998090
More
Less

3-ACETYL-1-(P-TOLYLSULFONYL)PYRROLE Usage And Synthesis

Synthesis

17639-64-4

108-24-7

106058-85-9

GENERAL STEPS: Acetic anhydride (0.44 mL, 4.7 mmol) was slowly added dropwise to a solution of dichloromethane (5.22 mL) containing aluminum chloride (896 mg, 6.7 mmol) at room temperature. After stirring the reaction mixture for 10 minutes, a solution of N-tosylpyrrole (400 mg, 1.81 mmol) in dichloromethane (0.9 mL) was added dropwise. Stirring of the reaction mixture was continued for 2 hours. Upon completion of the reaction, the mixture was poured into an ice-water mixture. The organic phase was separated and the aqueous phase was extracted with dichloromethane. The organic phases were combined, washed with 1N NaOH aqueous solution and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated to obtain the crude product. The crude product was washed with methanol and further purified to give 1-(1-toluenesulfonyl-1H-pyrrol-3-yl)ethanone (470 mg, 1.78 mmol, 99% yield) as a pure solid. Thin layer chromatography (TLC) analysis showed an Rf value of 0.5 (unfolding agent: hexane/ethyl acetate, 6/4). The structure of the product was confirmed by 1H NMR spectroscopy [24].

References

[1] Journal of Heterocyclic Chemistry, 2009, vol. 46, # 6, p. 1285 - 1295
[2] European Journal of Medicinal Chemistry, 2012, vol. 57, p. 391 - 397
[3] Patent: US2006/189555, 2006, A1. Location in patent: Page/Page column 10
[4] European Journal of Organic Chemistry, 2018, vol. 2018, # 1, p. 60 - 77
[5] Journal of Organic Chemistry, 1993, vol. 58, # 27, p. 7899 - 7902

3-ACETYL-1-(P-TOLYLSULFONYL)PYRROLESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Shanghai Sinch Parmaceuticals Tech. Co. Ltd.
Tel
+86-21-54098501
Email
sales@sinch.com.cn