ChemicalBook--->CAS DataBase List--->31686-94-9

31686-94-9

31686-94-9 Structure

31686-94-9 Structure
IdentificationBack Directory
[Name]

ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate
[CAS]

31686-94-9
[Synonyms]

Ethyl 4-(4-fluorophenyl)
Ethyl 4-fluoro-a,g-dioxo-benzenebutanoate
ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate
Benzenebutanoicacid,4-fluoro-α,γ-dioxo-,ethylester
4-(4-Fluoro-phenyl)-2,4-dioxo-butyric acid ethyl ester
Benzenebutanoic acid, 4-fluoro-α,γ-dioxo-, ethyl ester
Benzenebutanoic acid, 4-fluoro-.alpha.,.gaMMa.-dioxo-, ethyl ester
[Molecular Formula]

C12H11FO4
[MDL Number]

MFCD02672449
[MOL File]

31686-94-9.mol
[Molecular Weight]

238.21
Chemical PropertiesBack Directory
[Boiling point ]

360.9±22.0 °C(Predicted)
[density ]

1.241±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

6.00±0.25(Predicted)
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Spectrum DetailBack Directory
[Spectrum Detail]

ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate(31686-94-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Fluoroacetophenone

403-42-9

Diethyl oxalate

95-92-1

ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate

31686-94-9

Synthesis of ethyl 4-(4-fluorophenyl)-2,4-dioxobutanoate: In a 2L round-bottomed flask fitted with a reflux condenser tube and a CaCl2 drying tube, sodium metal (49.9 g, 2.17 mol, 3.0 eq.) was slowly dissolved in ethanol (1.0 L). After the resulting sodium ethanol solution was cooled to about 10°C, a mixture of 4-fluoroacetophenone (100.0 g, 0.72 mol) and diethyl oxalate (295 mL, 2.17 mol, 3.0 eq.) was slowly added. The reaction mixture was stirred for about 15 minutes and then placed in a refrigerator to stand overnight. Subsequently, the reaction mixture was poured into a mixture consisting of concentrated hydrochloric acid solution (300 mL) and ice (about 1 kg). The resulting precipitate was collected by filtration and washed with plenty of water and finally dried in a vacuum dryer using P2O5/KOH. The product was a light yellow powder, yield: 165.5 g (96% yield).

[References]

[1] Patent: WO2015/95337, 2015, A2. Location in patent: Paragraph 0030
[2] Synthetic Communications, 2013, vol. 43, # 1, p. 110 - 117
[3] Patent: WO2015/196071, A1. Location in patent: Paragraph 0520
[3] Patent: , 2015, . Location in patent: Paragraph 0520
[5] Patent: WO2017/40606, 2017, A1. Location in patent: Paragraph 0465
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