3-(Octadecyloxy)-5-[(5-methoxy-5-oxopentyl)oxy]phenylcarbamic acid phenylmethyl ester → 5-[3-Amino-5-(octadecyloxy)phenoxy]pentanoic acid methyl ester
Reaktionsgleichung
C1(COC(=O)[NH:10][C:11]2[CH:16]=[C:15]([O:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])[CH:14]=[C:13]([O:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH3:44])[CH:12]=2)C=CC=CC=1.[H][H]>[Pd].C1COCC1>[CH3:25][O:24][C:22](=[O:23])[CH2:21][CH2:20][CH2:19][CH2:18][O:17][C:15]1[CH:14]=[C:13]([O:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH3:44])[CH:12]=[C:11]([NH2:10])[CH:16]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of 8.9 g of 3-(octadecyloxy)-5-[(5-methoxy-5-oxopentyl)oxy]phenylcarbamic acid phenylmethyl ester and 1.5 g of 10% palladium on carbon in 250 ml of THF was stirred in a hydrogen atmosphere at room temperature for 2.5 hours. The catalyst was removed by filtration and the filtrate was concentrated at reduced pressure to a solid which was triturated with hexane and filtered to give 6.8 g (97% yield, mp 57°-59°) of 5-[3-amino-5-(octadecyloxy) phenoxy]pentanoic acid methyl ester.
Aufarbeitung
- customThe catalyst was removed by filtration
- concentrationthe filtrate was concentrated at reduced pressure to a solid which
- customwas triturated with hexane
- filtrationfiltered
Quellen und Nachweise
- ORD-Eintrag
- ord-727752e5ae1e479cb170b94bc5bd6d3b
- Quelldatensatz
- uspto-grants-1995_08
- Patentnummer
- US05446189
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