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HRID 36629Erstellt: 23. Oktober 2026

5,8,9,10-tetrahydro-4H-acephenanthrylen-7-one → 7-Hydroxy-7-methyl-7,8,9,10-tetrahydroacephenanthrene

https://huagongshe.com/de/reaction/36629

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5,8,9,10-tetrahydro-4H-acephenanthrylen-7-oneHCID 343954—
EduktHCID 178418373HCID 178418373—
LösungsmittelDiethyl EtherHCID 3283—
Produkt7-Hydroxy-7-methyl-7,8,9,10-tetrahydroacephenanthreneHCID 1993741762%

Reaktionsschritte

Methylmagnesium iodide in ether (1.51 mL of 3.0M) was added slowly to an ice bath cooled suspension of 7,8,9,10-tetrahydroacephenanthren-7-one (Scott, L. T.; Reinhardt, G.; Roelofs, N. H. J. Org. Chem. 1985, 50, 5886) (0.25 g, 1.13 mmol) in ether (10 mL). The bath was removed and the reaction mixture was allowed to warm to room temperature over 1.5 h. The reaction mixture was again cooled to 0° C. and quenched with saturated aqueous ammonium chloride solution. The reaction mixture was concentrated under reduced pressure. The resulting solid was purified via flash chromotography to give 0.17 g (62%) of a crystalline solid: MS (CI) m/e (%) 239 (M+H+, 100); 1H NMR (CDCl3, 300 MHz) δ 7.64 (d, 1H, J=8.0 Hz), 7.57 (s, 1H), 7.46 (t, 1H, J=8.4 Hz), 7.28 (d, 1H, J=6.6 Hz), 3.37 (s, 4H), 3.08 (m, 2H), 2.02 (m, 4H), 1.80 (s, 1H), 1.63 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05416089
Quelldatensatzuspto-grants-1995_05
ORD IDord-19b432aa4b7b4791a88a1dfa8ac4dd9e
Quellennotizuspto-grants-1995_05