Hydrochloric Acid → rac-(2R,3R)-3-amino-1,2,3,4-tetrahydronaphthalen-2-ol hydrochloride
Reaktionsgleichung
C1([C@@H](C)C([NH:10][C@@H:11]2[CH2:20][C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[CH2:13][C@H:12]2[OH:21])=O)C=CC=CC=1.[ClH:23]>>[ClH:23].[NH2:10][C@@H:11]1[CH2:20][C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH2:13][C@H:12]1[OH:21]Komponenten
3
Versuchsvorschrift
Trans-N-[(2R)-2-phenylpropanoyl]-3-amino-1,2,3,4-tetrahydro-2-naphthalenol, diastereoisomer A (183 mg) was refluxed in 6N aqueous hydrochloric acid (20 ml) for 4 hours. The reaction mixture was evaporated in vacuo and the residue taken up in water. The aqueous solution was washed with ethyl acetate and evaporated to give a white solid which was recrystallized from a methanol/ethyl acetate mixture to yield the title compound (99 mg).
Aufarbeitung
- customThe reaction mixture was evaporated in vacuo
- washThe aqueous solution was washed with ethyl acetate
- customevaporated
- customto give a white solid which
- customwas recrystallized from a methanol/ethyl acetate mixture
Quellen und Nachweise
- ORD-Eintrag
- ord-17b1acab53094edfb923d4202f0f915a
- Quelldatensatz
- uspto-grants-1992_04
- Patentnummer
- US05106861
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