HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2066952Erstellt: 27. Oktober 2026
Methyl iodide → (+/-)-4-Dimethylamino-2-methyl-4-phenylcyclohexanone
https://huagongshe.com/reaction/2066952
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | 4-(Dimethylamino)-4-phenylcyclohexan-1-one | HCID 11424492 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (+/-)-4-Dimethylamino-2-methyl-4-phenylcyclohexanone | HCID 67408596 | — |
Reaktionsschritte
Diisopropylamine (2.1 ml, 15 mmol) was provided in dry THF in argon and mixed with n-butyl lithium in hexane (2.5M, 6 ml, 15 mmol) at 30° C. The reaction mixture was cooled to −78° C. 4-(dimethylamino)-4-phenylcyclohexanone (2.17 g, 10 mmol), dissolved in 10 ml of dry THF, was added in drops to this solution within 10 min. The batch was stirred for 30 min at −78° C. and then mixed with methyl iodide (1.86 ml, 30 mmol). It was heated to RT and stirred for a further 18 h. The solvent was removed at the rotary evaporator and the residue taken up in DCM. Extraction was conducted with 1N HCl (3×30 ml). The aqueous phase was basified with 5N NaOH (20 ml) and extracted with DCM (3×30 ml). The combined organic phases were washed with H2O (2×10 ml) and dried over Na2SO4. The semisolid residue (1.2 g) obtained after removal of the solvent was recrystallised from ethyl acetate (1 ml).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08293758B2 |
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| Quelldatensatz | uspto-grants-2012_10 |
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| ORD ID | ord-0d735cbbb9c2411a9a3f0da231d40022 |
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| Quellennotiz | uspto-grants-2012_10 |
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