تفاعل #58955

ord-5f56c9601e4c46b8ba8c5ea72057fca1

معادلة التفاعل

Cn1ncc(C=O)c1-c1cccnc1
1-methyl-5-(3-pyridinyl)-1H-pyrazole-4-carbaldehyde
[H-].[Na+]
sodium hydride
CCOC(=O)CP(=O)(OCC)OCC
ethyl diethylphosphonoacetate
CN(C)C=O
N,N-dimethylformamide
CCOC(=O)/C=C/c1cnn(C)c1-c1cccnc1
ethyl (2E)-3-[1-methyl-5-(3-pyridinyl)-1H-pyrazol-4-yl]acrylate
المردود 75.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe mixture was extracted with ethyl acetate
  2. 2
    غسيلThe organic layer was washed with water
  3. 3
    تجفيفdried over anhydrous magnesium sulfate
  4. 4
    تركيزconcentrated
  5. 5
    أخرىRecrystallization of the residue from ethyl acetate-hexane

الإجراء التجريبي

A mixture of 1-methyl-5-(3-pyridinyl)-1H-pyrazole-4-carbaldehyde (750 mg), sodium hydride (60% in oil, 176 mg), ethyl diethylphosphonoacetate (1.08 g) and N,N-dimethylformamide (8 ml) was stirred at room temperature for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated. Recrystallization of the residue from ethyl acetate-hexane gave ethyl (2E)-3-[1-methyl-5-(3-pyridinyl)-1H-pyrazol-4-yl]acrylate (770 mg, 75%) as pale-yellow prism crystals. melting point: 159-160° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07423159B2uspto-grants-2008_09