Malonic Acid → Bis(2,4,6-trichlorophenyl) propanedioate

HRID 336638Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 336638
[C:1]([OH:7])(=[O:6])[CH2:2][C:3]([OH:5])=[O:4].[Cl:8][C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[C:11]([Cl:16])[C:10]=1O.P(Cl)(Cl)(Cl)=O>>[Cl:8][C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[C:11]([Cl:16])[C:10]=1[O:4][C:3](=[O:5])[CH2:2][C:1]([O:7][C:10]1[C:9]([Cl:8])=[CH:14][C:13]([Cl:15])=[CH:12][C:11]=1[Cl:16])=[O:6]

Komponenten

4

Edukt 3

HCID 867Malonic AcidHCID 69142,4,6-TrichlorophenolHCID 24813Phosphorus oxychloride

Produkt 1

HCID 2783450Bis(2,4,6-trichlorophenyl) propanedioateAusbeute 100,6 %

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

A mixture of malonic acid (20 g, 192 mmol), 2,4,6-trichlorophenol (72 g, 365 mmol), and phosphorus oxychloride (38 mL, 403.2 mmol) was stirred at reflux for 12 h. The reaction mixture was cooled to 70° C. and poured into ice water. The solid was collected by filtration, washed with water, and air-dried to give malonic acid bis-(2,4,6-trichloro-phenyl)ester (85 g, 95%). A solution of malonic acid bis-(2,4,6-trichloro-phenyl)ester (85 g, 183.6 mmol) and ethyl 3-aminocrotonate (26.1 g, 202 mmol) in bromobenzene (100 mL) was stirred at reflux for 50 min. The reaction mixture was cooled to 50° C. and diluted with EtOAc (260 mL). The solid was collected by filtration, washed with water, and air-dried, to give 4,6-dihydroxy-2-methyl nicotinic acid ethyl ester (31 g, 86%).

Aufarbeitung

  1. temperatureat reflux for 12 h
  2. filtrationThe solid was collected by filtration
  3. washwashed with water
  4. customair-dried

Quellen und Nachweise

ORD-Eintrag
ord-113ce640f03947d38b3c19c1edea4400
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08889698B2

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