2,2-Difluoropropionic acid

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2,2-Difluoropropionic acid Basic information
Uses Application
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
EINECS:
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 Structure
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)
Fp 25-30°C/5mm
storage temp. Inert atmosphere,Room Temperature
pka1.34±0.10(Predicted)
form powder to crystal
color White to Almost white
InChIInChI=1S/C3H4F2O2/c1-3(4,5)2(6)7/h1H3,(H,6,7)
InChIKeyPMWGIVRHUIAIII-UHFFFAOYSA-N
SMILESC(O)(=O)C(F)(F)C
CAS DataBase Reference373-96-6(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
MSDS Information
2,2-Difluoropropionic acid Usage And Synthesis
Uses2,2-Difluoropropionic acid is a useful research chemical.
Application2,2-Difluoropropionic acid is mainly used in biochemical research.
Chemical PropertiesWhite powder
Synthesis
Ethyl 2,2-Difluoropropionate

28781-85-3

2,2-Difluoropropionic acid

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
2,2-Difluoropropionic acid Preparation Products And Raw materials
Raw materialsEthyl 2,2-Difluoropropionate-->Propanoic acid, 2-bromo-2-fluoro-, ethyl ester-->Sodium hydroxide-->Ethanol
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