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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1262480Erstellt: 26. Oktober 2026

Sulfuric Acid → (4-Phenylcyclohexyl)methanol

https://huagongshe.com/reaction/1262480

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktEthyl AcetateHCID 8857—
EduktAluminium lithium hydrideHCID 21226445—
EduktHCID 178501033HCID 178501033—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHeptaneHCID 8900—
Produkt(4-Phenylcyclohexyl)methanolHCID 310060892,2%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

Dry tetrahydrofuran (THF) (420 ml) was added to lithiumaluminum hydride (11.1 g, 0.293 mol) and the mixture was vigorously agitated, followed by dropwise adding to the mixture, a solution obtained by dissolving trans-4-phenylcyclohexanecarboxylic acid methyl ester (II) (64.0 g, 0.293 mol) in THF (70 ml), while keeping the reaction temperature at 20° C. or lower. After completion of the dropwise addition, the reaction mixture was warmed up to 55° C., reacted for 2 hours and cooled, followed by adding ethyl acetate (12 ml) and water (100 ml), and then adding 18% sulfuric acid (350 ml) to form two separated layers of a tetrahydrofuran layer and an aqueous layer. n-Heptane (200 ml) was added to the former layer and the mixture was transferred into a separating funnel, followed by washing with water (500 ml), washing with 2% aqueous solution of sodium carbonate (500 ml), further washing with water till the aqueous layer became neutral, distilling off n-heptane and THF, recrystallizing solid as still residue from n-heptane (20 ml), filtering off the resulting 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
PatentnummerUS04452719
Quelldatensatzuspto-grants-1984_06
ORD IDord-cb836e5c00974092aa8e3dce0898ba1d
Quellennotizuspto-grants-1984_06