Water → trans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol
Reaktionsgleichung
[O:1]1[CH:11]2[CH:2]1[CH2:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]([OH:12])[C:9]=1[CH2:10]2.O.Cl(O)(=O)(=O)=[O:15].C(Cl)(Cl)Cl>O1CCCC1.CCOCC.C(=O)(O)[O-].[Na+]>[C:8]1([OH:12])[C:9]2[CH2:10][C@@H:11]([OH:1])[C@H:2]([OH:15])[CH2:3][C:4]=2[CH:5]=[CH:6][CH:7]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
A solution of 8.0 g of 5,6,7,8-tetrahydro-6,7-epoxy-1-naphthol in 100 ml of tetrahydrofuran is cooled to 0° C. and 20 ml of water and 0.5 ml of 70% perchloric acid are added. After 4 hours, a further 1.5 ml of acid is added and the solution is stirred for 16 hours at ambient temperature and diluted with 100 ml each of ether, 10% sodium bicarbonate and saturated salt solution. The aqueous layer is separated and washed with 150 ml of 1:1 ether-tetrahydrofuran. The organic phase is washed with saturated salt solution, dried and evaporated to give an oil which solidifies on trituration with chloroform. Recrystallization gives in two crops, 4.85 g of solid which is recrystallized from ethyl acetate to give 3.84 g, melting point 179.5°-181.5° C. Two further recrystallizations of a small sample give the analytical specimen, melting point 183°-184° C.
Aufarbeitung
- customThe aqueous layer is separated
- washwashed with 150 ml of 1:1 ether-tetrahydrofuran
- washThe organic phase is washed with saturated salt solution
- customdried
- customevaporated
- customto give an oil which
- customRecrystallization
Quellen und Nachweise
- ORD-Eintrag
- ord-1f98cbea66f64b34b71df0b5498e18ea
- Quelldatensatz
- uspto-grants-1977_06
- Patentnummer
- US04029676
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