ChemicalBook--->CAS DataBase List--->38107-10-7

38107-10-7

38107-10-7 Structure

38107-10-7 Structure
IdentificationBack Directory
[Name]

(4-PHENYL-THIAZOL-2-YL)-ACETIC ACID
[CAS]

38107-10-7
[Synonyms]

RARECHEM AL BO 0890
4-Phenyl-2-thiazoleacetic acid
2-Thiazoleacetic acid, 4-phenyl-
4-phenylthiazole-2-ylacetic acid
(4-PHENYL-THIAZOL-2-YL)-ACETIC ACID
2-(4-phenylthiazol-2-yl)acetic acid
(4-Phenyl-1,3-thiazol-2-yl)acetic acid
2-(4-phenyl-1,3-thiazol-2-yl)acetic Acid
[Molecular Formula]

C11H9NO2S
[MDL Number]

MFCD05177043
[MOL File]

38107-10-7.mol
[Molecular Weight]

219.26
Chemical PropertiesBack Directory
[Melting point ]

90-91℃
[density ]

1.329
[storage temp. ]

2-8°C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

4-Phenyl-2-thiazoleacetic Acid is a reactant used to prepare heterocyclic acetamide and benzamide derivatives as β3-adrenergic receptor agonists.
[Synthesis]

2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETONITRILE

41381-89-9

(4-PHENYL-THIAZOL-2-YL)-ACETIC ACID

38107-10-7

General procedure for the synthesis of 4-phenyl-2-thiazoleacetic acid from 2-(4-phenylthiazol-2-yl)acetonitrile: To a solution of 2-(4-phenylthiazol-2-yl)acetonitrile (130 mg, 0.649 mmol) in ethanol (1.5 mL) was added a 5 M sodium hydroxide solution (0.389 mL, 1.947 mmol). The reaction mixture was heated to reflux for 1 hour. Upon completion of the reaction, the reaction solution was diluted with 1 M aqueous hydrochloric acid solution (5 mL) and subsequently extracted five times with chloroform (10 mL). The organic layers were combined and dried with magnesium sulfate. The solvent was removed by evaporation under reduced pressure. The residue was purified by silica gel column chromatography (eluent ratio chloroform:methanol:acetic acid = 10:1:0.1) to afford 4-phenyl-2-thiazoleacetic acid (77.2 mg, 54% yield) as a brown oil.1H-NMR (DMSO-d6) data were as follows: δ (ppm) 4.13 (s, 2H), 7.30-7.37 (m, 1H). 7.39-7.47 (m, 2H), 7.90-7.97 (m, 2H), 8.04 (s, 1H), 12.81 (brs, 1H).

[References]

[1] Patent: EP2351744, 2011, A1. Location in patent: Page/Page column 60
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