Benzyl Bromide → 5-(Decyloxy)-2-(phenylmethoxy)benzoic acid methyl ester
Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:9]=[C:8]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH:7]=[CH:6][C:5]=1[OH:21].[CH2:23](Br)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:9]=[C:8]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH:7]=[CH:6][C:5]=1[O:21][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1Komponenten
3
Versuchsvorschrift
The reaction of 5-(decyloxy)-2-hydroxybenzoic acid methyl ester with benzyl bromide under conditions described in Example 59 gave 5-(decyloxy)-2-(phenylmethoxy)benzoic acid methyl ester (81% yield, mp 32°-34°).
Quellen und Nachweise
- ORD-Eintrag
- ord-3ec2de622eb543b08c8d21e2c5c1ecbe
- Quelldatensatz
- uspto-grants-1994_03
- Patentnummer
- US05298652
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