Benzoic Acid → HCID 56984157, Verbindung

HRID 1395214

Reaktionsgleichung

Reaktionsgleichung von HRID 1395214
[C:1]([CH:6]1[CH2:11][CH2:10][CH:9]([CH:12]=O)[CH2:8][CH2:7]1)([CH2:4][CH3:5])([CH3:3])[CH3:2].[C:14]([C:19](=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH3:20])([O:16][CH2:17][CH3:18])=[O:15].C(O)(=O)C1C=CC=CC=1>C1(C)C=CC=CC=1>[CH2:17]([O:16][C:14](=[O:15])[C:19]([CH3:20])=[CH:12][CH:9]1[CH2:8][CH2:7][CH:6]([C:1]([CH2:4][CH3:5])([CH3:2])[CH3:3])[CH2:11][CH2:10]1)[CH3:18]

Komponenten

5

Versuchsvorschrift

A mixture of 46.3 g of 4-tert.amyl-cyclohexane-1-carboxaldehyde, 92.3 g of (α-carbethoxy-ethylidene)-triphenyl-phosphorane and 7.6 g of benzoic acid in 250 ml of toluene is heated at reflux for 3.5 hours under nirogen gasification and the toluene is evaporated. The oily-crystalline residue is dissolved in 1600 ml of methanol/water (4:1) and exhaustively extracted with hexane. The combined hexane extracts are washed with sodium carbonate solution and water, dried over sodium sulphate and evaporated. By distillation there is obtained pure 3-(4-tert.amyl-cyclohexyl)-2-methyl-acrylic acid ethyl ester of boiling point 113°-115° C./0.03 Torr.

Aufarbeitung

  1. temperatureis heated
  2. temperatureat reflux for 3.5 hours under nirogen gasification
  3. customthe toluene is evaporated
  4. dissolutionThe oily-crystalline residue is dissolved in 1600 ml of methanol/water (4:1)
  5. extractionexhaustively extracted with hexane
  6. washThe combined hexane extracts are washed with sodium carbonate solution and water
  7. dry with materialdried over sodium sulphate
  8. customevaporated
  9. distillationBy distillation there

Quellen und Nachweise

ORD-Eintrag
ord-b5aefe35b1e94d719a364b9f83476dfd
Quelldatensatz
uspto-grants-1980_05
Patentnummer
US04202894

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