ChemicalBook--->CAS DataBase List--->4320-91-6

4320-91-6

4320-91-6 Structure

4320-91-6 Structure
IdentificationBack Directory
[Name]

2H-1,2,3 TRIAZOLE-2-ACETIC ACID
[CAS]

4320-91-6
[Synonyms]

AP8Impurity
2H-1,2,3 TRIAZOLE-2-ACETIC ACID
2-(2H-1,2,3-triazol-2-yl)acetic acid
[Molecular Formula]

C4H5N3O2
[MDL Number]

MFCD03840810
[MOL File]

4320-91-6.mol
[Molecular Weight]

127.1
Chemical PropertiesBack Directory
[Boiling point ]

344.0±44.0 °C(Predicted)
[density ]

1.53±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

2?+-.0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2H-1,2,3 TRIAZOLE-2-ACETIC ACID(4320-91-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

2H-1,2,3 TRIAZOLE-2-ACETIC ACID ETHYL ESTER

4320-90-5

2H-1,2,3 TRIAZOLE-2-ACETIC ACID

4320-91-6

The general procedure for the synthesis of 2H-2-acetic acid-1,2,3-triazole-1,2,3-triazole from ethyl 2-(2H-1,2,3-triazol-2-yl)acetate was as follows: 1. Preparation of 2H-1,2,3-triazol-2-ylacetic acid: a solution of lithium hydroxide monohydrate (2.5 g, 60 mmol) in water (15 mL) was added to a solution of ethyl 2-(2H-1,2,3-triazol-2-yl)acetate (7.8 g, 50 mmol), and the reaction was stirred for 18 h at room temperature. 2. Upon completion of the reaction, the reaction mixture was acidified with 2M hydrochloric acid (150 mL) followed by extraction with dichloromethane (150 mL x 3). 3. The organic phases were combined, dried over magnesium sulfate and concentrated under reduced pressure to afford 2H-2-acetic acid-1,2,3-triazole as a white solid in 81% (5.2 g) yield. 4. 4. Product characterization: 1H NMR (400 MHz, CDCl3) δ: 5.35 (s, 2H), 7.72 (s, 2H); LRMS APCI m/z 128 [M + H]+.

[References]

[1] Patent: WO2006/123242, 2006, A1. Location in patent: Page/Page column 35
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