Potassium Hydroxide → [5-(3-Methylbutoxy)-2-propylphenylthio] fumaric acid

HRID 1606106Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1606106
[CH3:1][CH:2]([CH3:16])[CH2:3][CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]([CH2:13][CH2:14][CH3:15])=[C:10]([SH:12])[CH:11]=1.[OH-].[K+].[K+].[C:20]([C:25]([O-:27])=[O:26])#[C:21][C:22]([OH:24])=[O:23]>O>[CH3:1][CH:2]([CH3:16])[CH2:3][CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]([CH2:13][CH2:14][CH3:15])=[C:10]([S:12]/[C:21](=[CH:20]\[C:25]([OH:27])=[O:26])/[C:22]([OH:24])=[O:23])[CH:11]=1

Komponenten

5

Versuchsvorschrift

A solution of 95.7 parts of 5-(3-methylbutoxy)-2-propylthiophenol, 54 parts of potassium hydroxide and 73 parts of acetylene dicarboxylic acid mono potassium salt in 350 parts of water was refluxed for 40 minutes and cooled. The mixture was filtered through Whatman 54 filter paper to remove an oil residue and the filtrate was acidified to pH 1 with concentrated hydrochloric acid. The resulting yellow precipitate was collected, washed with water and dried in vacuo to give 67.8 parts of the desired product as a yellow powder, mp 121° - 129°C Crystallization from 15% ethanol-water afforded pure [5-(3-methylbutoxy)-2-propylphenylthio] fumaric acid, m.p. 131° - 133°C.

Aufarbeitung

  1. temperaturecooled
  2. filtrationThe mixture was filtered through Whatman 54
  3. filtrationfilter paper
  4. customto remove an oil residue
  5. customThe resulting yellow precipitate was collected
  6. washwashed with water
  7. customdried in vacuo
  8. customto give
  9. custom67.8 parts of the desired product as a yellow powder, mp 121° - 129°C Crystallization from 15% ethanol-water afforded pure [5-(3-methylbutoxy)-2-propylphenylthio] fumaric acid, m.p. 131° - 133°C.

Quellen und Nachweise

ORD-Eintrag
ord-ee2496d876034faaab063a1b7e507f35
Quelldatensatz
uspto-grants-1976_04
Patentnummer
US03952013

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