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4-(DIFLUOROMETHOXY)ACETOPHENONE

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4-(DIFLUOROMETHOXY)ACETOPHENONE Basic information
Product Name:4-(DIFLUOROMETHOXY)ACETOPHENONE
Synonyms:AKOS B016264;AKOS BBS-00000545;4-(DIFLUOROMETHOXY)ACETOPHENONE;1-(4-DIFLUOROMETHOXY-PHENYL)-ETHANONE;ART-CHEM-BB B016264;1-[4-(difluoromethoxy)phenyl]ethan-1-one;4'-(Difluoromethoxy)acetophenone 98%;4'-(Difluoromethoxy)acetophenone98%
CAS:83882-67-1
MF:C9H8F2O2
MW:186.16
EINECS:281-174-7
Product Categories:
Mol File:83882-67-1.mol
4-(DIFLUOROMETHOXY)ACETOPHENONE Structure
4-(DIFLUOROMETHOXY)ACETOPHENONE Chemical Properties
Melting point 18-19°C
Boiling point 70-72°C 0,5mm
density 1.191±0.06 g/cm3(Predicted)
refractive index 1.4930 to 1.4970
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Light orange to Yellow to Green
λmax252nm(EtOH)(lit.)
CAS DataBase Reference83882-67-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
Hazard Note Irritant
HS Code 2914790090
MSDS Information
4-(DIFLUOROMETHOXY)ACETOPHENONE Usage And Synthesis
Chemical Reactivity4-(DIFLUOROMETHOXY)ACETOPHENONE is a chemical compound that contains the difluoromethoxy group. It has been shown to be a nitrogen-containing heterocycle, which makes it an important part of many pyridine derivatives. The cyclic molecule is also known as 1,2-difluoroethanone.
Synthesis
Sodium chlorodifluoroacetate

1895-39-2

4'-Hydroxyacetophenone

99-93-4

4-(DIFLUOROMETHOXY)ACETOPHENONE

83882-67-1

To a stirred solution of 4-hydroxyacetophenone (5.0 g, 36.76 mmol) in N,N-dimethylformamide (DMF, 50 mL) was added sodium 2-chloro-2,2-difluoroacetate (6.2 g, 40.44 mmol) followed by sodium hydroxide (NaOH, 1.76 g, 44.11 mmol). The reaction mixture was stirred at 100 °C for 14 hours. After completion of the reaction, the mixture was diluted with cold water and the product was extracted with ethyl acetate (EtOAc). The organic layers were combined, dried with anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography using a 20-30% ethyl acetate/hexane solvent mixture to afford the target compound 1-(4-difluoromethoxyphenyl)ethanone (3.5 g, 51.0% yield) as a colorless liquid.1H NMR (400 MHz, DMSO-d6): δ 8.05-8.01 (m, 2H), 7.59-7.22 (m 3H), 2.50 (s, 3H); LC-MS: m/z 187.0 [M+H]+.

References[1] Patent: WO2018/165520, 2018, A1. Location in patent: Page/Page column 215-216
4-(DIFLUOROMETHOXY)ACETOPHENONE Preparation Products And Raw materials
Raw materialsSodium chlorodifluoroacetate-->4'-Hydroxyacetophenone-->Sodium hydroxide-->N,N-Dimethylformamide
Preparation Products2'-(DIFLUOROMETHOXY)ACETOPHENONE 98-->(1E)-1-[4-(difluoromethoxy)phenyl]ethanone oxime
Tag:4-(DIFLUOROMETHOXY)ACETOPHENONE(83882-67-1) Related Product Information
4-(TRIFLUOROMETHOXY)BENZOYL ACETONITRILE 4'-(Trifluoromethoxy)acetophenone 4-(Difluoromethoxy)acetophenone (DIFLUOROMETHOXY)BENZENE 2'-(DIFLUOROMETHOXY)ACETOPHENONE 98,2'-(Difluoromethoxy)acetophenone 98% 4-(Trifluoromethoxy)phenacyl bromide 4-(Difluoromethoxy)phenacyl bromide 1-(4-DIFLUOROMETHOXY-3-METHOXY-PHENYL)-4,4,4-TRIFLUORO-BUTANE-1,3-DIONE (4-BROMO-PHENYL)-(4-TRIFLUOROMETHOXY-PHENYL)-METHANONE [3,5-DI(TRIFLUOROMETHYL)PHENYL][4-(TRIFLUOROMETHOXY)PHENYL]METHANONE 1-(4-DIFLUOROMETHOXY-PHENYL)-4,4,4-TRIFLUORO-BUTANE-1,3-DIONE SALOR-INT L122912-1EA SALOR-INT L124400-1EA 5-CHLORO-1-OXO-1-(4-TRIFLUOROMETHOXYPHENYL)PENTANE SALOR-INT L125121-1EA SALOR-INT L121606-1EA SALOR-INT L126047-1EA [2-(Trifluoromethoxy)phenyl][4-(trifluoromethoxy)phenyl]methanone