Basic information Safety Supplier Related

2,2-DIFLUOROPENT-4-ENOIC ACID

Basic information Safety Supplier Related

2,2-DIFLUOROPENT-4-ENOIC ACID Basic information

Product Name:
2,2-DIFLUOROPENT-4-ENOIC ACID
Synonyms:
  • 2,2-DIFLUOROPENT-4-ENOIC ACID
  • 4-Pentenoic acid, 2,2-difluoro-
  • 2,2-Difluoro-4-pentenoicacid,97%
  • 2,2-Difluoropent-4-enoic acid,98% (stabilized with MEHQ)
CAS:
55039-89-9
MF:
C5H6F2O2
MW:
136.1
Mol File:
55039-89-9.mol
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2,2-DIFLUOROPENT-4-ENOIC ACID Chemical Properties

Boiling point:
56-58°C/3mm
Density 
1.218
Flash point:
55℃
storage temp. 
2-8°C
pka
1.27±0.10(Predicted)
Appearance
Light brown to brown Liquid
Water Solubility 
Immiscible with water.
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Safety Information

Hazard Codes 
Xi
RIDADR 
3265
HazardClass 
IRRITANT
HazardClass 
8
PackingGroup 
HS Code 
2916199590
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2,2-DIFLUOROPENT-4-ENOIC ACID Usage And Synthesis

Uses

2,2-Difluoro-4-pentenoic acid is involved in the iodolactonization reaction to give the corresponding gamma- lactone, which is converted to prepare prepare 5-hydroxy-3,3-difluoropiperidine.

Synthesis

118337-48-7

55039-89-9

The general procedure for synthesizing 2,2-difluoro-4-pentenoic acid from allyl chlorodifluoroacetate is as follows: in Example 9, 100.0 g (0.59 mol) of allyl chlorodifluoroacetate, 42.2 g (0.65 mol) of zinc powder activated by the Fieser and Fieser methods, 96.7 g (0.88 mol) of trimethylchlorosilane and 400 mL of anhydrous acetonitrile were added to a glass autoclave and a trace amount of iodine was added as initiator. The reaction mixture was heated at 100 °C for 48 hours. Upon completion of the reaction, the precipitated zinc salt was removed by filtration and the filtrate was hydrolyzed with water. Subsequently, the reaction mixture was alkalized with 2N NaOH solution. The dark brown aqueous phase was extracted with pentane and then acidified with semi-concentrated hydrochloric acid before the product was extracted with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated in a rotary evaporator and the residue was vacuum distilled. A final 59.4 g (74% yield) of the colorless oily product 2,2-difluoro-4-pentenoic acid was obtained with a boiling point of 73°-75°C/15.6 mbar.

References

[1] Chemical Research in Toxicology, 1995, vol. 8, # 5, p. 671 - 682
[2] Patent: US4892962, 1990, A

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