Basic information Safety Supplier Related

1-(4-FLUORO-PHENYL)-BUTAN-1-ONE

Basic information Safety Supplier Related

1-(4-FLUORO-PHENYL)-BUTAN-1-ONE Basic information

Product Name:
1-(4-FLUORO-PHENYL)-BUTAN-1-ONE
Synonyms:
  • 1-Butanone, 1-(4-fluorophenyl)-
  • Butyrophenone, 4'-fluoro-
  • p-Fluorobutyrophenone
  • 1-(4-FLUORO-PHENYL)-BUTAN-1-ONE
  • 1-(4-Fluorophenyl)-1-butanone
  • p-Fluorophenylpropyl ketone
  • 4'-Fluorobutyrophenone 98%
  • 2-methyl-1-propen-1-ol
CAS:
582-83-2
MF:
C10H11FO
MW:
166.19
EINECS:
209-492-3
Mol File:
582-83-2.mol
More
Less

1-(4-FLUORO-PHENYL)-BUTAN-1-ONE Chemical Properties

Melting point:
38 °C
Boiling point:
102 °C
Density 
1.050±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Water Solubility 
Insoluble in water.
CAS DataBase Reference
582-83-2(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2914790090
More
Less

1-(4-FLUORO-PHENYL)-BUTAN-1-ONE Usage And Synthesis

Uses

4'-fluorobutyrophenone derivatives is used in the preparation of its derivatives that includes haloperidol, haloanisone, triperidol, methylperidide, haloperidide and dipiperone.

Synthesis

462-06-6

141-75-3

582-83-2

In a 500 mL four-necked flask, n-butyryl chloride (55.5 g, 0.52 mol) was dissolved in ethylene dichloride (250 mL), stirred well, and cooled to about 10°C. Fluorobenzene (52.1 g, 0.57 mol) was dissolved in 100 mL of ethylene dichloride, prepared as a solution and then slowly added dropwise to the n-butyryl chloride solution. After the dropwise addition was completed, the reaction mixture was heated and the reaction process was monitored by thin layer chromatography (TLC) or gas chromatography (GC). Upon completion of the reaction, the reaction solution was poured into a mixture of dilute hydrochloric acid and ice, stirred for 1 hour, and left to stratify. The organic phase was separated and washed sequentially with water and saturated sodium carbonate solution. The solvent was removed by distillation under reduced pressure, and the fraction at 102~105°C/9 mmHg was collected to give 77.8 g of 4-fluorobutyrophenone in 90% yield and 99.0% purity.

References

[1] Patent: CN105384707, 2016, A. Location in patent: Paragraph 0003; 0026
[2] Patent: WO2018/165520, 2018, A1. Location in patent: Page/Page column 159
[3] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 781,785
[4] Archiv der Pharmazie, 1963, vol. 296, p. 324 - 336
[5] Patent: CN104974053, 2017, B. Location in patent: Paragraph 0062; 0063

1-(4-FLUORO-PHENYL)-BUTAN-1-ONESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Shijiazhuang Sdyano Fine Chemical Co., Ltd.
Tel
0311-89250318 031166536426
Email
master@sjzsdyn.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com