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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494568Generated: October 25, 2026

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

https://huagongshe.com/reaction/494568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexane, (bromomethyl)-HCID 137636—
ReactantMethyl alpha-methylbenzeneacetateHCID 569653—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-cyclohexyl-2-methyl-2-phenylpropanateHCID 6887455184.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538105B2
Source datasetuspto-grants-2009_05
ORD IDord-ddfb2fe1ac2648dd89fd37fd398aae52
Source noteuspto-grants-2009_05