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Water → 8-Methoxy-3,7-dimethyl-octa-1,6-dien-3-ol

HRID 437497
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 437497
[CH3:1][O:2][CH:3](C)[C:4]([CH3:11])=[CH:5][CH2:6][CH2:7][C:8](=[O:10])[CH3:9].[CH:13]([Mg]Cl)=[CH2:14].O>O1CCCC1>[CH3:1][O:2][CH2:3][C:4]([CH3:11])=[CH:5][CH2:6][CH2:7][C:8]([CH3:9])([OH:10])[CH:13]=[CH2:14]
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Komponenten

5

Edukt 3

HCID 962WaterHCID 53786798HCID 53786798, VerbindungHCID 178461836HCID 178461836, Verbindung

Produkt 1

HCID 539177528-Methoxy-3,7-dimethyl-octa-1,6-dien-3-olAusbeute 85 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

141 g (0.9 mole) of 7-methoxy-6-methyl-oct-5-en-2-one are added to 1 mole of a 1.5 normal solution of vinyl-magnesium chloride in tetrahydrofuran, at below 20° C, in the course of one hour. After a further 2 hours' reaction, hydrolysis is carried out with 100 ml of water, whilst cooling with ice. After a homogeneous salt suspension has formed, the salt and the tetrahydrofuran solution are separated by filtering or centrifuging. The tetrahydrofuran is distilled off under reduced pressure and the reaction product which remains is purified by fractional distillation. 164 g of 8-methoxy-3,7-dimethyl-octa-1,6-dien-3-ol (yield 85%) are obtained. Boiling point 73°-75° C/0.01 bar; nD25 = 1.4676.

Aufarbeitung

  1. customAfter a further 2 hours' reaction, hydrolysis
  2. temperaturewhilst cooling with ice
  3. customAfter a homogeneous salt suspension has formed
  4. customthe salt and the tetrahydrofuran solution are separated
  5. filtrationby filtering
  6. distillationThe tetrahydrofuran is distilled off under reduced pressure
  7. distillationthe reaction product which remains is purified by fractional distillation

Quellen und Nachweise

ORD-Eintrag
ord-6664a19cec2f4dc6a0695b347a1f976c
Quelldatensatz
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04031141

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