Thiofenchone → (+-)-Fenchone
Reaktionsgleichung
[CH3:1][C:2]1([CH3:11])[C:8](=S)[C:6]2([CH3:10])[CH2:7][CH:3]1[CH2:4][CH2:5]2.C[O:13]C1C=CC([Te](C2C=CC(OC)=CC=2)=O)=CC=1>>[CH3:1][C:2]1([CH3:11])[C:8](=[O:13])[C:6]2([CH3:10])[CH2:7][CH:3]1[CH2:4][CH2:5]2Komponenten
3
Versuchsvorschrift
Thiofenchone (23 mg, 0.14 mmol) was reacted with bis-(p-methoxyphenyl)telluroxide for 42 h. Fenchone (5 mg, 23%) νmax 1965,1930,1875,1742,1465,1385 and 1025 cm-1 was obtained after p.l.c. (petroleum ether-ethyl acetate 20:1). A low yield was obtained due to volatility of the product. Sulphur and bis-(p-methoxyphenyl)telluride were, however, isolated in 75 and 81% yields respectively.
Quellen und Nachweise
- ORD-Eintrag
- ord-46f188a4f2c349e29009205b486c5935
- Quelldatensatz
- uspto-grants-1983_01
- Patentnummer
- US04370497
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