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METHYL 2,6-DIFLUOROBENZOATE

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METHYL 2,6-DIFLUOROBENZOATE Basic information

Product Name:
METHYL 2,6-DIFLUOROBENZOATE
Synonyms:
  • 2,6-DIFLUOROBENZOIC ACID METHYL ESTER
  • METHYL 2,6-DIFLUOROBENZOATE
  • RARECHEM AL BF 0212
  • Methyl 2,6-difluorobenzoate 98%
  • Methyl2,6-difluorobenzoate98%
  • Benzoic acid, 2,6-difluoro-, Methyl ester
  • Methyl 2,6-difluorobenzoate, 97%+
  • 2,6-difluorobenzoate
CAS:
13671-00-6
MF:
C8H6F2O2
MW:
172.13
EINECS:
642-850-0
Product Categories:
  • Aromatic Esters
  • C8 to C9
  • Carbonyl Compounds
  • Esters
Mol File:
13671-00-6.mol
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METHYL 2,6-DIFLUOROBENZOATE Chemical Properties

Boiling point:
203-204 °C (lit.)
Density 
1.281 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.476(lit.)
Flash point:
203 °F
storage temp. 
Sealed in dry,Room Temperature
form 
fused solid
color 
White to off white
BRN 
1948618
CAS DataBase Reference
13671-00-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/38
Safety Statements 
26-36-26/37
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29163990

MSDS

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METHYL 2,6-DIFLUOROBENZOATE Usage And Synthesis

Uses

Methyl 2,6-difluorobenzoate may be used in the synthesis of 9-hydroxy-13-(2,6-difluorophenyl)-3H-dibenzo[b,i]xanthen-3-one and 2,6-difluorobenzohydroxamic acid.

General Description

Methyl 2,6-difluorobenzoate is a fluorinated aromatic ester. It can be synthesized from 2,6-difluorobenzoic acid via esterification with methanol.

Synthesis

67-56-1

385-00-2

13671-00-6

GENERAL METHOD: A catalytic amount of concentrated H2SO4 (0.1 mmol) was added to a methanol (50 mL) solution of 2,6-difluorobenzoic acid (1.0 mmol) and the mixture was heated to reflux for 6 hours. Upon completion of the reaction, the reaction mixture was cooled to room temperature. Subsequently, saturated NaHCO3 solution (50 mL) was added to the reaction mixture to neutralize the acidic conditions, and then the product was extracted with ethyl acetate (2 x 50 mL). The organic phases were combined, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure to give pure methyl 2,6-difluorobenzoate.

References

[1] Organic Process Research and Development, 2016, vol. 20, # 2, p. 233 - 241
[2] Medicinal Chemistry Research, 2016, vol. 25, # 4, p. 627 - 643
[3] Patent: WO2011/59610, 2011, A1. Location in patent: Page/Page column 101-102
[4] Patent: WO2013/71865, 2013, A1. Location in patent: Page/Page column 25
[5] Patent: CN103102349, 2017, B. Location in patent: Paragraph 0147-0149

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