Dimethyl [1-acetyl-4,8,12-trimethyltrideca-3,7,11-trienyl]phosphonate → [1-Acetyl-4,8,12-trimethyltrideca-3,7,11-trienyl]phosphonic acid

HRID 488155

Reaktionsgleichung

Reaktionsgleichung von HRID 488155
O=C(CCC=C(C)CCC=C(C)CCC=C(C)C)CP(=O)(OC)OC.[C:26]([CH:29]([P:45](=[O:50])([O:48]C)[O:46]C)[CH2:30][CH:31]=[C:32]([CH3:44])[CH2:33][CH2:34][CH:35]=[C:36]([CH3:43])[CH2:37][CH2:38][CH:39]=[C:40]([CH3:42])[CH3:41])(=[O:28])[CH3:27]>>[C:26]([CH:29]([P:45](=[O:46])([OH:48])[OH:50])[CH2:30][CH:31]=[C:32]([CH3:44])[CH2:33][CH2:34][CH:35]=[C:36]([CH3:43])[CH2:37][CH2:38][CH:39]=[C:40]([CH3:42])[CH3:41])(=[O:28])[CH3:27]

Komponenten

3

Versuchsvorschrift

This compound was prepared exactly by the method described in Step 2 of Example 2 except that dimethyl [2-oxo-6,10,14-trimethylpentadeca-5,9,13-trienyl]phosphonate was replaced by dimethyl [1-acetyl-4,8,12-trimethyltrideca-3,7,11-trienyl]phosphonate. Thereby was obtained title compound as a colorless gum.

Aufarbeitung

  1. customThis compound was prepared exactly by the method

Quellen und Nachweise

ORD-Eintrag
ord-01ad4f021690429b82a6dad23d0828f0
Quelldatensatz
uspto-grants-1994_03
Patentnummer
US05298655

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