ChemicalBook--->CAS DataBase List--->838892-95-8

838892-95-8

838892-95-8 Structure

838892-95-8 Structure
IdentificationBack Directory
[Name]

5-(Bromomethyl)-2-methylthiazole
[CAS]

838892-95-8
[Synonyms]

5-(Bromomethyl)-2-methylthiazole
Thiazole, 5-(bromomethyl)-2-methyl-
5-(BROMOMETHYL)-2-METHYL-1,3-THIAZOLE
[Molecular Formula]

C5H6BrNS
[MDL Number]

MFCD04035605
[MOL File]

838892-95-8.mol
[Molecular Weight]

192.08
Chemical PropertiesBack Directory
[Boiling point ]

231.0±15.0 °C(Predicted)
[density ]

1.629±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

2.69±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

(2-Methyl-1,3-thiazol-5-yl)Methanol

56012-38-5

5-(Bromomethyl)-2-methylthiazole

838892-95-8

Step 2: Synthesis of 2-methyl-5-hydroxymethylthiazole At room temperature, 2-methyl-5-hydroxymethylthiazole (12 g, 0.1 mol) was dissolved in dichloromethane (500 mL) and the resulting solution was cooled to 0-5 °C in an ice water bath. Subsequently, triphenylphosphine (52 g, 0.2 mol) and carbon tetrabromide (66 g, 0.2 mol) were added to the cooled mixture in batches. After the addition was completed, the reaction mixture was allowed to warm up naturally to room temperature and stirred continuously at this temperature for 2 hours. Upon completion of the reaction, the mixture was concentrated and purified by silica gel column chromatography (eluent ratio of petroleum ether:ethyl acetate = 2:1), resulting in a yellow solid product (3.3 g, overall yield in two steps: 15%).

[References]

[1] Patent: EP3181554, 2017, A1. Location in patent: Paragraph 0092
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