Reaktionsgleichung
C[O:2][C:3](=[O:20])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]([NH:16]C(=O)C)=[CH:12][CH:11]=1.[ClH:21]>>[ClH:21].[NH2:16][C:13]1[CH:12]=[CH:11][C:10]([O:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][C:3]([OH:20])=[O:2])=[CH:15][CH:14]=1Komponenten
3
Reaktionsbedingungen
- Temperatur
- 10 °C
Versuchsvorschrift
A mixture of 6-(4-Acetylaminophenoxy)hexanoic acid methyl ester 19 (290 grams, 1.04 mol) in concentrated hydrochloric acid (7.12 L) was refluxed for 48 hours. Excess concentrated hydrochloric acid was distilled off in vacuum and filtered hot. The mixture was cooled to 10° C., filtered and dried give pure 20 (150 g, 55.6%) as a brown powder. The melting point was found to be 155-160° C.
Aufarbeitung
- temperaturewas refluxed for 48 hours
- distillationExcess concentrated hydrochloric acid was distilled off in vacuum
- filtrationfiltered hot
- filtrationfiltered
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-aaaf3cd83c2b4643bc5b4bb389e8ae5a
- Quelldatensatz
- uspto-grants-2010_04
- Patentnummer
- US07691364B2
Verknüpfte Notizen
Wird geladen…