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HRID 494568Erstellt: 24. Oktober 2026

Cyclohexane, (bromomethyl)- → Methyl 3-cyclohexyl-2-methyl-2-phenylpropanate

https://huagongshe.com/de/reaction/494568

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexane, (bromomethyl)-HCID 137636—
EduktMethyl alpha-methylbenzeneacetateHCID 569653—
EduktLithium HexamethyldisilazideHCID 2733832—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 3-cyclohexyl-2-methyl-2-phenylpropanateHCID 6887455184,5%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A solution of 2-phenyl-propionic acid methyl ester (3.0 g, 18.27 mmol) in tetrahydrofuran (25 mL) at −78° C. was treated dropwise with the lithium hexamethyldisilazide (21.9 mL, 1M in tetrahydrofuran, 21.9 mmol) and stirred for 1 hour. Bromomethyl-cyclohexane (3.09 mL, 21.92 mmol) was added to the reaction and the reaction was allowed to warm to 25° C. and stirred for 18 hours. The solvent was removed in vacuo and the residue was partitioned between water and ethyl acetate. The aqueous phase was extracted three times with ethyl acetate and the ethyl acetate layers were combined, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with hexane, then 2.5% ethyl acetate in hexane, and 5% ethyl acetate in hexane to give the title compound (4.02 g, 84%). 1H NMR (300 MHz, CDCl3): δ ppm 1.11 (m, 10H) 1.55 (m, 4H) 1.80 (m, 1H) 2.04 (m, 1H) 3.64 (m, 3H) 7.29 (m, 5H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538105B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-ddfb2fe1ac2648dd89fd37fd398aae52
Quellennotizuspto-grants-2009_05