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Rac. benzyl 2,6,10-trimethylundeca-4,8-dien-1yl ether → 2,6,10-Trimethylundecan-1-ol

HRID 1277536
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Reaktionsgleichung

Reaktionsgleichung von HRID 1277536
[CH3:1][CH:2]([CH2:12][CH:13]=[CH:14][CH:15]([CH3:22])[CH2:16][CH:17]=[CH:18][CH:19]([CH3:21])[CH3:20])[CH2:3][O:4]CC1C=CC=CC=1.[H][H]>C(OCC)(=O)C>[CH3:1][CH:2]([CH2:12][CH2:13][CH2:14][CH:15]([CH3:22])[CH2:16][CH2:17][CH2:18][CH:19]([CH3:21])[CH3:20])[CH2:3][OH:4]
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Komponenten

4

Edukt 2

HCID 70572593Rac. benzyl 2,6,10-trimethylundeca-4,8-dien-1yl etherHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 125714642,6,10-Trimethylundecan-1-olAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A mixture of 0.15 g (0.5 mmole) of rac. benzyl 2,6,10-trimethylundeca-4,8-dien-1yl ether, 0.1 g of 5% by weight palladiumon 95% by weight carbon and 10 ml. of ethyl acetate was stirred in an atmosphere of hydrogen for 16 hours at room temperature. The catalyst was filtered and the filtrate was concentrated in vacuo. The oily residue was dissolved in 10 ml. of ethyl acetate and rehydrogenated over 0.1 g of 5% palladium on carbon, for 5 hours at room temperature. The catalyst was again filtered and the filtrate was concentrated in vacuo. The residue wasevaporatively distilled giving 0.092 g (86%) of rac. 2,6,10-trimethylundecan-1-ol as a colorless oil, b.p. 100°-105° C. (bath temperature) (0.02 mm Hg.).

Aufarbeitung

  1. filtrationThe catalyst was filtered
  2. concentrationthe filtrate was concentrated in vacuo
  3. dissolutionThe oily residue was dissolved in 10 ml
  4. filtrationThe catalyst was again filtered
  5. concentrationthe filtrate was concentrated in vacuo
  6. distillationThe residue wasevaporatively distilled

Quellen und Nachweise

ORD-Eintrag
ord-338e1aaaed5647cc955363a97ce22c34
Quelldatensatz
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04277610

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