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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1248095Erstellt: 24. Oktober 2026

Sulfuric Acid → (4-Phenylcyclohexyl)methanol

https://huagongshe.com/de/reaction/1248095

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktEthyl AcetateHCID 8857—
EduktAluminium lithium hydrideHCID 21226445—
EduktHCID 178501033HCID 178501033—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4-Phenylcyclohexyl)methanolHCID 310060892,2%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

Dry tetrahydrofuran (THF)(420 ml) was added to lithium aluminum hydride (11.1 g, 0.293 mol), and while the mixture was vigorously agitated, there was dropwise added a soltuion obtained by dissolving trans-4-phenylcyclohexanecarboxylic acid methyl ester (II) (64.0 g, 0.293 mol) in THF (70 ml), at a reaction temperature kept at 20° C. or lower. After completion of the addition, the reaction mixture was warmed up to 55° C., followed by reacting it for 2 hours and cooling. Ethyl acetate (12 ml) and water (100 ml) were then added, followed by adding a 1N aqueous solution of sulfuric acid (350 ml) to dissolve inorganic matter, separating the resulting organic layer and aqueous layer from one another, adding n-heptane (200 ml) to extract the organic layer, washing the extract solution with water 500 ml), then washing with a 2% aqueous solution of Na2CO3, further washing with water until the aqueous layer became neutral, distilling off n-heptane and THF, recrystallizing the resulting solid as residue from n-heptane (20 ml), filtering off crystals and drying to obtain 4-phenylcyclohexylmethanol (III) (51.4 g). M.P. 47.3°~48.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04522741
Quelldatensatzuspto-grants-1985_06
ORD IDord-4c92742c633b4b8cbb9918259bce6434
Quellennotizuspto-grants-1985_06