تفاعل #1357

ord-9622eb5e098b43e1961ca5b2635ecda8

معادلة التفاعل

O=Cc1ccccc1Br
2-bromobenzaldehyde
CCC(CC)(C(=O)O)C(O)C(=O)O
diethylmaloic acid
C1CCNCC1
piperidine
CC(=O)O
acetic acid
CCC(CC=Cc1ccccc1Br)(C(=O)O)C(=O)O
desired product
المردود 90.0%
CCC(CC=Cc1ccccc1Br)(C(=O)O)C(=O)O
2-bromobenzylidene diethylmalonic acid
المردود 90.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA 500-ml three-necked round flask (Dean & Stark) equipped with a stirring bar
  2. 2
    غسيلby washing with 100 ml of water two times
  3. 3
    تجفيفThe organic phase was dried over anhydrous Na2SO4
  4. 4
    تركيزThe solvent was concentrated under reduced pressure
  5. 5
    تركيزthe concentrate of a orange liquid
  6. 6
    workup.DISTILLATIONwas distilled under reduced pressure

الإجراء التجريبي

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%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723640uspto-grants-1998_03