Acetic Anhydride → HCID 13298061, Verbindung
Reaktionsgleichung
[C:1]1([C:7]([C:19]2[CH:24]=[CH:23][C:22]([O:25][CH2:26][CH2:27][N:28]([CH3:30])[CH3:29])=[CH:21][CH:20]=2)([OH:18])[CH:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:9][CH2:10][OH:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:31](OC(=O)C)(=[O:33])[CH3:32]>>[C:31]([O:11][CH2:10][CH2:9][CH:8]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)([C:19]1[CH:20]=[CH:21][C:22]([O:25][CH2:26][CH2:27][N:28]([CH3:30])[CH3:29])=[CH:23][CH:24]=1)[OH:18])(=[O:33])[CH3:32]Komponenten
Reaktionsbedingungen
- Temperatur
- 90 °C
Versuchsvorschrift
The reaction is performed under dry conditions. 40.5 g of either (RR,SS)- or (RS,SR)-1,2-diphenyl-1-[4-[2-(N,N-dimethylamino)ethoxy]phenyl]butane-1,4-diol and 150 ml of acetic acid anhydride are placed in a flask. The temperature is raised to 90° C., where it is kept until the primaryOH-group is completely acetylated. [4-acetoxy-1,2-diphenyl-1-[4-[2-(N ,N-dimethylamino)ethoxy]phenyl]butan-1-ol is obtained as intermediate: m.p. of the (RR,SS)-isomer pair is 97°-9° C⟧ While stirring the reaction mixture, 30 ml of acetyl chloride in 50 ml of aceticacid anhydride are added at 90° C. The stirring is continued at thistemperature for 2 h. The solvent is evaporated. Then 1M sodium carbonate solution is added in excess, after which the product is extracted in toluene. The solution is dried over sodium sulfate, and the solvent is evaporated. The yield of the pure isomer mixture (Z:E 2:1) is quantitative. The m.p. of the (Z)-isomer is 88° -90° C. prepared from the corresponding (Z)-alcohol by refluxing in acetic acid.
Quellen und Nachweise
- ORD-Eintrag
- ord-5ec2212abf4a41f5a8fbad6115943d13
- Quelldatensatz
- uspto-grants-1996_02
- Patentnummer
- US05491173
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