Acetic Acid → 2-Bromobenzylidene diethylmalonic acid

HRID 1585184

Reaktionsgleichung

Reaktionsgleichung von HRID 1585184
[Br:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[CH2:10]([C:12]([CH2:21][CH3:22])([C:18]([OH:20])=[O:19])[CH:13]([OH:17])C(O)=O)[CH3:11].N1CCCCC1.C(O)(=[O:31])C>CCOCC.C1C=CC=CC=1>[Br:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[CH:22][CH2:21][C:12]([CH2:10][CH3:11])([C:13]([OH:17])=[O:31])[C:18]([OH:20])=[O:19]

Komponenten

7

Edukt 4

HCID 176Acetic AcidHCID 8082PiperidineHCID 811292-BromobenzaldehydeHCID 21642744Diethylmaloic acid

Produkt 1

HCID 670846452-Bromobenzylidene diethylmalonic acidAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 241BenzeneLösungsmittelHCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

A 500-ml three-necked round flask (Dean & Stark) equipped with a stirring bar, a Dimroth condenser and a thermometer was charged with 74.0 g (400 mmol) of 2-bromobenzaldehyde, 70.48 g (440 mmol) of diethylmaloic acid, 1.6 ml of piperidine, 4.8 ml of acetic acid and 80 ml of benzene. The mixture was subjected to azeotoropic dehydration for 7 hours in an oil bath of 110° C. under a nitrogen atmosphere. After the reaction was completed, the reaction mixture was cooled to room temperature and 300 ml of ether was added, followed by washing with 100 ml of water two times. The organic phase was dried over anhydrous Na2SO4. The solvent was concentrated under reduced pressure and the concentrate of a orange liquid was distilled under reduced pressure to obtain 117.2 g of the desired product as a yellow liquid (yield: 90%).

Aufarbeitung

  1. customA 500-ml three-necked round flask (Dean & Stark) equipped with a stirring bar
  2. washby washing with 100 ml of water two times
  3. dry with materialThe organic phase was dried over anhydrous Na2SO4
  4. concentrationThe solvent was concentrated under reduced pressure
  5. concentrationthe concentrate of a orange liquid
  6. distillationwas distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-8e68f9139f8a4cc999c73805ba663c34
Quelldatensatz
uspto-grants-1999_08
Patentnummer
US05936053

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