3-Nitrobenzaldehyde → Ethyl 2-Methyl-3-(3-Nitrophenyl)propenoate

HRID 66802

反応式

HRID 66802 の反応式
C1(P(C2C=CC=CC=2)(C2C=CC=CC=2)=[C:8]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH3:9])C=CC=CC=1.[N+:27]([C:30]1[CH:31]=[C:32]([CH:35]=[CH:36][CH:37]=1)[CH:33]=O)([O-:29])=[O:28]>C1C=CC=CC=1>[CH3:9][C:8](=[CH:33][C:32]1[CH:35]=[CH:36][CH:37]=[C:30]([N+:27]([O-:29])=[O:28])[CH:31]=1)[C:10]([O:12][CH2:13][CH3:14])=[O:11]

参加物

4

反応物 2

HCID 74493-NitrobenzaldehydeHCID 79792Ethyl 2-(triphenylphosphoranylidene)propionate

生成物 1

HCID 54141471Ethyl 2-Methyl-3-(3-Nitrophenyl)propenoate

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

To a stirred slurry of 79.8 g. of triphenyl(1[ethoxycarbonyl]ethylidene)phosphorane in 300 ml. of benzene was added 30.2 g. of 3-nitrobenzaldehyde and the resulting mixture was heated under reflux overnight. The reaction mixture was cooled and the solvent was removed by evaporation in vacuo. The residue was extracted with 300 ml. of isopropyl ether. The isopropyl ether solution was filtered, and the filtrate was evaporated in vacuo. The residue was distilled under reduced pressure, giving 37.6 g. of the title product, b.p. 147°-162° C./0.25 mm Hg. The NMR spectrum (in CDCl3) showed absorptions at 1.4 (t), 2.1 (d), 4.3 (q), 7.4 (m) and 8.1 (m) ppm.

後処理

  1. temperatureunder reflux overnight
  2. temperatureThe reaction mixture was cooled
  3. customthe solvent was removed by evaporation in vacuo
  4. extractionThe residue was extracted with 300 ml
  5. filtrationThe isopropyl ether solution was filtered
  6. customthe filtrate was evaporated in vacuo
  7. distillationThe residue was distilled under reduced pressure
  8. customgiving 37.6 g

出典と根拠

ORDレコード
ord-eadc72b7dc9343619d37a611cd20b587
出典データセット
uspto-grants-1982_08
特許番号
US04343813

関連ノート

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