Phenylacetone → 8-Acetyl-8-(2-methylphenyl)-12-hydroxyheptadecanoic Acid
Reaktionsgleichung
CC1C=CC=CC=1CC(=O)C.C1(CC(=O)C)C=CC=CC=1.CC1C=CC=CC=1C(CCCC(OCC1C=CC=CC=1)CCCCC)C(=O)C.[C:50]([C:53]([C:82]1[CH:87]=[CH:86][CH:85]=[CH:84][C:83]=1[CH3:88])([CH2:65][CH2:66][CH2:67][CH:68]([O:74]CC1C=CC=CC=1)[CH2:69][CH2:70][CH2:71][CH2:72][CH3:73])[CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][C:60]([O:62]CC)=[O:61])(=[O:52])[CH3:51].C(C(C1C=CC=CC=1C)(CCCC(OCC1C=CC=CC=1)CCCCC)CCCCCCC(O)=O)(=O)C.C(C(CCCC(O)CCCCC)CCCCCC(C1C=CC=CC=1C)C(O)=O)(=O)C>>[C:50]([C:53]([C:82]1[CH:87]=[CH:86][CH:85]=[CH:84][C:83]=1[CH3:88])([CH2:65][CH2:66][CH2:67][CH:68]([OH:74])[CH2:69][CH2:70][CH2:71][CH2:72][CH3:73])[CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][C:60]([OH:62])=[O:61])(=[O:52])[CH3:51]Komponenten
7
Edukt 6
Produkt 1
Versuchsvorschrift
By following the procedures described in Example 3, but substituting (2-methyphenyl) acetone for the phenylacetone employed in Step C, there are obtained successively from that point: 3-(2-methylphenyl)-7-benzyloxy-2-dodecanone (Step C); ethyl 8-acetyl-8-(2-methylphenyl)-12-benzyloxyheptadecanoate (Step D); 8-acetyl-8-(2-methylphenyl)-12-benzyloxyheptadecanoic acid (Step E); and 8-acetyl-(2-methylphenyl)-12-hydroxyheptadecanoic acid (Step F).
Aufarbeitung
- customare obtained successively from that point
Quellen und Nachweise
- ORD-Eintrag
- ord-1cf35223ac974e00afcce910c6a7e6b9
- Quelldatensatz
- uspto-grants-1977_11
- Patentnummer
- US04059602
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