StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Formic Acid → Valeric acid, 2,2,4-trimethyl-

HRID 1589584
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1589584
[CH3:1][CH:2]([CH:4](O)[CH:5]([CH3:7])[CH3:6])[CH3:3].S(=O)(=O)(O)O.[CH:14]([OH:16])=[O:15]>>[CH3:1][C:2]([CH3:3])([CH2:4][CH:5]([CH3:7])[CH3:6])[C:14]([OH:16])=[O:15]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 284Formic Acid2×HCID 1118Sulfuric AcidHCID 117522,4-Dimethyl-3-pentanol

Produkt 1

HCID 3013951Valeric acid, 2,2,4-trimethyl-

Versuchsvorschrift

2,4-Dimethyl-3-pentanol (29 g, 0.25 mole), dissolved in formic acid (98%, 46 g, 1 mole), was added dropwise over one hour to a rapidly-stirred, ice-cooled mixture of formic acid (98%, 3 ml) and concentrated sulfuric acid (270 ml). During the addition the reaction mixture foamed vigorously and was stirred for a further one hour at 10°-20° C. The mixture was poured on to ice (1 kg) and the resulting solution extracted with hexanes (3×200 ml). The combined organic phases were extracted with 2N potassium hydroxide (2×200 ml) plus ice (50 g) and the aqueous extracts washed with hexanes (100 ml). The aqueous phase was then acidified (pH 2) and the product extracted into hexanes (3×200 ml). After washing with saturated sodium chloride and drying (MgSO4), the solution was evaporated under reduced pressure and the residue distilled to give 2,2,4-trimethylpentanoic acid (36 g).

Aufarbeitung

  1. additionwas added dropwise over one hour to a rapidly-stirred, ice-
  2. temperaturecooled
  3. additionDuring the addition the reaction mixture
  4. extractionthe resulting solution extracted with hexanes (3×200 ml)
  5. extractionThe combined organic phases were extracted with 2N potassium hydroxide (2×200 ml) plus ice (50 g)
  6. washthe aqueous extracts washed with hexanes (100 ml)
  7. extractionthe product extracted into hexanes (3×200 ml)
  8. washAfter washing with saturated sodium chloride
  9. dry with materialdrying (MgSO4)
  10. customthe solution was evaporated under reduced pressure
  11. distillationthe residue distilled

Quellen und Nachweise

ORD-Eintrag
ord-69ff2acdbf564f79a80c7de2ca67e365
Quelldatensatz
uspto-grants-1986_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04571345

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion