Hydrochloric Acid → HCID 86718436, Verbindung
Reaktionsgleichung
[I:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=2)(O)[CH3:9])=[CH:4][CH:3]=1.C(OC(=O)C)(=O)C.Cl>>[I:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([C:11]2[CH:12]=[CH:13][C:14]([O:17][CH3:18])=[CH:15][CH:16]=2)=[CH2:9])=[CH:6][CH:7]=1Komponenten
4
Versuchsvorschrift
The side chain used in example 5 (1-(4-iodophenyl)-1-(4-methoxyphenyl)ethanol) (1.25 g, 2.86 mmol) was treated with acetic anhydride (13.49 ml, 143 mmol) and HCl conc (1.042 ml, 34.3 mmol) and the reaction mixture was stirred at room temperature overnight. The reaction mixture was filtered. The precipitate was washed well with n-heptane then dried in vacuo to obtain the title compound as white solid.
Aufarbeitung
- filtrationThe reaction mixture was filtered
- washThe precipitate was washed well with n-heptane
- customthen dried in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-cb69c39dcf5b474c9fec2c3cbd483d58
- Quelldatensatz
- uspto-grants-2014_10
- Patentnummer
- US08859535B2
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