2,2-Difluoropropionic acid
2,2-Difluoropropionic acid Basic information
- Product Name:
- 2,2-Difluoropropionic acid
- Synonyms:
-
- 2,2-DIFLUOROPROPIONIC ACID
- 2,2-Difluoropropanoic acid
- 2,2-Difluoropropionic acid 97%
- Propanoic acid, 2,2-difluoro-
- CAS:
- 373-96-6
- MF:
- C3H4F2O2
- MW:
- 110.06
- Product Categories:
-
- Carboxylic Acids
- Chemical Synthesis
- Fluorinated Building Blocks
- Organic Building Blocks
- Organic Fluorinated Building Blocks
- Other Fluorinated Organic Building Blocks
- Alkyl Fluorinated Building Blocks
- Building Blocks
- C1 to C5
- Carbonyl Compounds
- C1 to C5
- Carbonyl Compounds
- Carboxylic Acids
- Mol File:
- 373-96-6.mol
2,2-Difluoropropionic acid Chemical Properties
- Melting point:
- 38-45 °C
- Boiling point:
- 25-30 °C/5 mmHg
- Density
- 1.316±0.06 g/cm3(Predicted)
- Flash point:
- 25-30°C/5mm
- storage temp.
- Inert atmosphere,Room Temperature
- form
- powder to crystal
- pka
- 1.34±0.10(Predicted)
- color
- White to Almost white
- InChI
- InChI=1S/C3H4F2O2/c1-3(4,5)2(6)7/h1H3,(H,6,7)
- InChIKey
- PMWGIVRHUIAIII-UHFFFAOYSA-N
- SMILES
- C(O)(=O)C(F)(F)C
- CAS DataBase Reference
- 373-96-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,C
- Risk Statements
- 34-36
- Safety Statements
- 26-36/37/39
- RIDADR
- 3261
- WGK Germany
- 3
- HazardClass
- 8
- PackingGroup
- III
- HS Code
- 29159000
2,2-Difluoropropionic acid Usage And Synthesis
Uses
2,2-Difluoropropionic acid is a useful research chemical.
Uses
2,2-Difluoropropionic acid is mainly used in biochemical research.
Chemical Properties
White powder
Synthesis
28781-85-3
373-96-6
The general procedure for synthesizing 2,2-difluoropropionic acid from ethyl 2,2-difluoropropionate was as follows: referring to Example G38, ethyl 2,2-difluoropropionate (1.2 g, 8.8 mmol) was dissolved in ethanol (26 mL), followed by the slow addition of 2N aqueous sodium hydroxide solution (26 mL). The reaction mixture was stirred at 0 °C, then gradually warmed to room temperature and continued stirring for 14 hours. Upon completion of the reaction, the reaction mixture was acidified to pH < 7 with 2N hydrochloric acid and then extracted with ether. The organic phases were combined, dried over anhydrous sodium sulfate and subsequently concentrated under reduced pressure to give 2,2-difluoropropionic acid (0.90 g, 92% yield). The product was an oil with the following 1H-NMR (CDCl3) data: δ 1.85 (3H, t, J = 19.0 Hz), 6.21 (1H, br s).
References
[1] Patent: EP1402900, 2004, A1
[2] Patent: US2004/53973, 2004, A1
[3] Journal of Organic Chemistry USSR (English Translation), 1981, vol. 17, p. 1260 - 1263
[4] Zhurnal Organicheskoi Khimii, 1981, vol. 17, # 7, p. 1417 - 1420
[5] Journal of Organic Chemistry USSR (English Translation), 1982, vol. 18, p. 1597 - 1601
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