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

Acetic Acid → Ethyl 3-methylpent-4-enoate

HRID 638099
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 638099
[CH2:1](O)[CH:2]=[CH:3][CH3:4].[C:6]([O:14]CC)([O:11][CH2:12][CH3:13])(OCC)[CH3:7].C(O)(=O)CC.C(O)(=O)C>CCOCC.O>[CH3:4][CH:3]([CH:2]=[CH2:1])[CH2:7][C:6]([O:11][CH2:12][CH3:13])=[O:14]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 176Acetic AcidHCID 1032Propionic AcidHCID 200242-Buten-1-olHCID 66221Triethyl orthoacetate

Produkt 1

HCID 12476290Ethyl 3-methylpent-4-enoate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel
HCID 3283
Diethyl Ether
Lösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A stirred mixture of 36.06 g of crotyl alcohol, 162.2 g of triethyl orthoacetate and 2.22 g of propionic acid was slowly heated to 100° C. (1.25 hours), stirred and heated at 100°-115° C. for 1 hour, at 115°-145° C. for 2.5 hours, then at 145°-155° C. for 6 hours. The mixture was cooled in an ice bath and treated with 50 ml of glacial acetic acid and 50 ml of water. The mixture was stirred at room temperature for 45 minutes, diluted with ether, extracted with saturated sodium bicarbonate solution, then with brine and dried (MgSO4). The solvent was evaporated under reduced pressure and the residue was distilled under reduced pressure to give ethyl 3-methyl-4-pentenoate (3A), as a colorless liquid, b.p.: 88°-91° C. (60 Torr.).

Aufarbeitung

  1. temperatureheated at 100°-115° C. for 1 hour, at 115°-145° C. for 2.5 hours
  2. temperatureThe mixture was cooled in an ice bath
  3. stirringThe mixture was stirred at room temperature for 45 minutes
  4. extractionextracted with saturated sodium bicarbonate solution
  5. dry with materialwith brine and dried (MgSO4)
  6. customThe solvent was evaporated under reduced pressure
  7. distillationthe residue was distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-6dda0d16ea4b430cb5b81c4f833711f2
Quelldatensatz
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04560401

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion