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2-(Chloromethyl)thiophene

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2-(Chloromethyl)thiophene Basic information

Product Name:
2-(Chloromethyl)thiophene
Synonyms:
  • THIOPHENE, 2-(CHLOROMETHYL)-
  • 2-(chloromethyl)thiophene
  • 2-(Chloromethyl)thiophene###765-50-4
  • 2-(Chloromethyl)thiophene, 33% w/w solution in toluene
  • 2-(Chloromethyl)thiophene ISO 9001:2015 REACH
  • Thenyl chloride
CAS:
765-50-4
MF:
C5H5ClS
MW:
132.61
EINECS:
212-150-6
Product Categories:
  • Sulfur
  • API Intermediate
Mol File:
765-50-4.mol
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2-(Chloromethyl)thiophene Chemical Properties

Boiling point:
80-81 °C(Press: 18 Torr)
Density 
1.243±0.06 g/cm3(Predicted)
storage temp. 
Amber Vial, -20°C Freezer
solubility 
Acetonitrile, Chloroform
form 
Oil
color 
Colourless
CAS DataBase Reference
765-50-4(CAS DataBase Reference)
NIST Chemistry Reference
Thiophene, 2-(chloromethyl)-(765-50-4)
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Safety Information

RIDADR 
1993
HazardClass 
3
PackingGroup 
HS Code 
2933399990
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2-(Chloromethyl)thiophene Usage And Synthesis

Chemical Properties

Colorless Liquid

Synthesis

636-72-6

765-50-4

The general procedure for the synthesis of 2-chloromethylthiophene from 2-thiophenemethanol was as follows: 2-thiophenemethanol (5,58 g, 509 mmol) and pyridine (60 g, 763 mmol) were dissolved in 600 mL of anhydrous dichloromethane at 0 °C, and thionyl chloride was added slowly and dropwise. The reaction mixture was stirred at 0°C for 1 hour, then brought to room temperature and continued to stir overnight. Upon completion of the reaction, the reaction was quenched by the addition of 500 mL of water. The organic layer was separated and the aqueous layer was extracted twice with 300 mL of dichloromethane. The organic layers were combined and washed sequentially with 600 mL of 5% aqueous sodium bicarbonate and 300 mL of brine. The organic layer was dried with anhydrous sodium sulfate and concentrated to give 40 g of 2-chloromethylthiophene (6) as an oil in 60% yield.

References

[1] European Journal of Medicinal Chemistry, 2001, vol. 36, # 11-12, p. 873 - 886
[2] European Journal of Pharmaceutical Sciences, 2002, vol. 16, # 1-2, p. 15 - 28
[3] European Journal of Organic Chemistry, 2014, vol. 2014, # 11, p. 2365 - 2370
[4] Tetrahedron, 1998, vol. 54, # 25, p. 6999 - 7012
[5] Synthetic Communications, 2005, vol. 35, # 15, p. 2079 - 2083

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