Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 2-Phenylcyclohexanone | HCID 95592 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 178521548 | HCID 178521548 | — |
Reaktionsschritte
Tetrahydrofuran (200 ml) was dropwise added into a 1 l capacity three-necked flask containing lithiumaluminum hydride (9.9 g, 0.26 mol), at 0° C., followed by sufficiently suspending these materials, dropwise adding a solution of phenylcyclohexanone (91.3 g, 0.52 mol) in tetrahydrofuran (200 ml), agitating the mixture at room temperature for 2 hours, again cooling it down to 0° C., dropwise adding ethyl acetate (20 ml), further adding dilute hydrochloric acid (100 ml), removing insolubles in the resulting reaction solution by suction-filtration, adding ethyl acetate (100 ml) to the filtrate for extraction, three times washing the resulting organic layer with water (100 ml), drying it over magnesium sulfate, filtering off magnesium sulfate, concentrating the residue under reduced pressure to obtain white crystals (98.5 g), recrystallizing from alcohol and drying to obtain 4-trans-phenylcyclohexanol (55 g). M.P.: 117°-119° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05202055 |
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| Quelldatensatz | uspto-grants-1993_04 |
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| ORD ID | ord-11c110657b6642af8635907f02453028 |
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| Quellennotiz | uspto-grants-1993_04 |
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