Methanol → 4-[7-(2-Ethylbutylcarbamoyl)naphth-1-ylmethyl]-3-methoxybenzoic acid
Reaktionsgleichung
O.[OH-].[Li+].[CH2:4]([CH:6]([CH2:34][CH3:35])[CH2:7][NH:8][C:9]([C:11]1[CH:20]=[C:19]2[C:14]([CH:15]=[CH:16][CH:17]=[C:18]2[CH2:21][C:22]2[CH:31]=[CH:30][C:25]([C:26]([O:28]C)=[O:27])=[CH:24][C:23]=2[O:32][CH3:33])=[CH:13][CH:12]=1)=[O:10])[CH3:5].CO.O1CCCC1>O>[CH2:34]([CH:6]([CH2:4][CH3:5])[CH2:7][NH:8][C:9]([C:11]1[CH:20]=[C:19]2[C:14]([CH:15]=[CH:16][CH:17]=[C:18]2[CH2:21][C:22]2[CH:31]=[CH:30][C:25]([C:26]([OH:28])=[O:27])=[CH:24][C:23]=2[O:32][CH3:33])=[CH:13][CH:12]=1)=[O:10])[CH3:35]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of lithium hydroxide monohydrate (150 mg) in water (4 ml) was added to a solution of methyl 4-(7-(2-ethylbutylcarbamoyl)naphth-1-ylmethyl)-3-methoxybenzoate (310 mg) in 1:1 methanol:tetrahydrofuran (15 ml). The mixture was stirred for 18 h. After most of the solvent was evaporated, water (7 ml) was added. The mixture was acidified with 1N hydrochloric acid and the precipitate was filtered, triturated with 25 ml of 10:1 ether:methanol, ground to a powder and vacuum dried at 100° C for 12 h to give 4-[7-(2-ethylbutylcarbamoyl)naphth-1-ylmethyl]-3-methoxybenzoic acid (221 mg, 74%) as a colorless solid; mp 198.0°-199.0° C.
Aufarbeitung
- customAfter most of the solvent was evaporated
- additionwater (7 ml) was added
- filtrationthe precipitate was filtered
- customtriturated with 25 ml of 10:1 ether
- dry with materialmethanol, ground to a powder and vacuum dried at 100° C for 12 h
Quellen und Nachweise
- ORD-Eintrag
- ord-5e8943b8fa9e42aea30f3b1eea7ac6a7
- Quelldatensatz
- uspto-grants-1992_03
- Patentnummer
- US05095038
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