Hydrochloric Acid → 4-[(3-Phenylpropyl)amino]benzoic acid
Reaktionsgleichung
[C:1]1([CH2:7][CH2:8][CH2:9][NH:10][C:11]2[CH:21]=[CH:20][C:14]([C:15]([O:17]CC)=[O:16])=[CH:13][CH:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[K+].C(O)C.O.Cl>O>[C:1]1([CH2:7][CH2:8][CH2:9][NH:10][C:11]2[CH:12]=[CH:13][C:14]([C:15]([OH:17])=[O:16])=[CH:20][CH:21]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 10 g. of ethyl p-[(3-phenylpropyl)amino]benzoate (prepared as described in Example 26), 10 g. of KOH and 200 ml. of ethanol-water (9:1) is refluxed for 4 hours. The mixture is acidified while hot with concentrated hydrochloric acid, diluted with water, cooled and filtered to give off-white crystals. Recrystallization from ethanol gives off-white crystals, m.p. 162°-163° C.
Aufarbeitung
- additionA mixture of 10 g
- temperaturecooled
- filtrationfiltered
- customto give off-white crystals
- customRecrystallization from ethanol
- customgives off-white crystals, m.p. 162°-163° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-ba8d7a0c2e884974a47cab8607644399
- Quelldatensatz
- uspto-grants-1980_01
- Patentnummer
- US04185115
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