3,5-difluorobenzophenone

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3,5-difluorobenzophenone manufacturers

3,5-difluorobenzophenone Basic information
Product Name:3,5-difluorobenzophenone
Synonyms:3,5-DIFLUOROBENZOPHENONE;3,5-Difluorobenzophenone 97%;3,5-Difluorobenzophenone97%;3,5-DIFLUOROBENZOPHENONE, 98+%;(3,5-Difluorophenyl)(phenyl)methanone;Methanone, (3,5-difluorophenyl)phenyl-
CAS:179113-89-4
MF:C13H8F2O
MW:218.2
EINECS:642-490-4
Product Categories:
Mol File:179113-89-4.mol
3,5-difluorobenzophenone Structure
3,5-difluorobenzophenone Chemical Properties
Melting point 57-59°C
Boiling point 117°C 5mm
density 1.239±0.06 g/cm3(Predicted)
Fp 116-118°C/5mm
storage temp. 2-8°C
form crystalline solid
color Yellow
BRN 7919206
InChIInChI=1S/C13H8F2O/c14-11-6-10(7-12(15)8-11)13(16)9-4-2-1-3-5-9/h1-8H
InChIKeyPNRLNUIMFIMZLI-UHFFFAOYSA-N
SMILESC(C1=CC(F)=CC(F)=C1)(C1=CC=CC=C1)=O
CAS DataBase Reference179113-89-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
HazardClass IRRITANT
HS Code 2914390090
MSDS Information
ProviderLanguage
ALFA English
3,5-difluorobenzophenone Usage And Synthesis
PreparationSynthesis of 3,5-Difluorobenzophenone: Prior to acylations, 3,5-difluorobenzoic acid was reacted with freshly distilled thionyl chloride and catalytic amounts of DMF(2 drops). After two hours at 55 °C, the excess thionyl chloride was distilled between 75 and 77 °C. The acid halide was then fractionally distilled at 174 °C, and recovery was generally around 75%. To a 50 mL round bottom flask, equipped with a gas inlet, addition funnel, condenser, and drying tube, were added 3.01 g (22.6 mmol) of AlCl3. A mixture of 3.62 g (20.5 mmol) 3,5-difluorobenzoyl chloride and 8.01 g (102.5 mmol) benzene was added dropwise to the AlCl3. The reaction mixture was stirred for 4 hours, before heating to 75 °C. After 16 hours the reaction mixture was quenched by pouring into acidic ice water, followed by addition of 300 mL of chloroform, and transferring to a separatory funnel. The layers were separated and the organic layer was washed with 5 wt. % bicarbonate, distilled water, and then dried with MgSO4 and the solvents were removed, via rotary evaporation, leaving an off-white solid. The crude material was recrystallized from aqueous ethanol to afford (3.00 g, 67 %) of a crystalline white solid with a m.p. 58-59 °C (lit.21 m.p. 57-58 °C); 1H NMR (300 MHz, CDCl3, δ) 7.04 (tt, 1H, J = 8.4, 2.4 Hz), 7.31 (m, 2H), 7.51 (m, 2H), 7.63 (tt, 1H, J = 7.5, 1.2 Hz), 7.78 (m, 2H)
3,5-difluorobenzophenone Preparation Products And Raw materials
Raw materialsBenzenecarbothioic acid, S-phenyl ester-->3,5-Difluorophenylboronic acid-->Benzoic acid pentafluorophenyl ester, BzOPfp
Tag:3,5-difluorobenzophenone(179113-89-4) Related Product Information
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