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765-50-4

765-50-4 Structure

765-50-4 Structure
IdentificationMore
[Name]

2-(Chloromethyl)thiophene
[CAS]

765-50-4
[Synonyms]

2-(chloromethyl)thiophene
THIOPHENE, 2-(CHLOROMETHYL)-
[EINECS(EC#)]

212-150-6
[Molecular Formula]

C5H5ClS
[MDL Number]

MFCD00797972
[Molecular Weight]

132.61
[MOL File]

765-50-4.mol
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[RIDADR ]

1993
[HazardClass ]

3
[PackingGroup ]

[HS Code ]

2933399990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Thiophene(SIV) (9CI)-->Thiophene, 2,2'-(1,2-ethanediyl)bis--->2-Thiophenemethanol-->Chloromethyl methyl ether-->Methanesulfonyl chloride-->2-Thiophenecarboxylic acid-->2-Thiophenecarboxaldehyde-->2,5-bis(chloroMethyl)thiophene-->2-Methylthiophene-->Formaldehyde
[Preparation Products]

Thiophen-2-ylmethyl-phosphonic acid diethyl ester-->2-(b-(2-Thienyl)vinyl)benzoicacid-->2-[2-(2-thienyl)ethyl]benzoic acid-->4-Oxo-9,10-dihydro-4H-benzo(4,5)-cyclohepta-(1,2b)thiophene-->2-Thiophenecarboxaldehyde-->2-Thiophenemethanethiol-->beta-(2-Thienyl)-DL-alanine
Hazard InformationBack Directory
[Chemical Properties]

Colorless Liquid
[Synthesis]

2-Thiophenemethanol

636-72-6

2-(Chloromethyl)thiophene

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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