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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132104Generated: October 25, 2026

Cyclohexanone → 1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanol

https://huagongshe.com/reaction/132104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantPentaneHCID 8003—
Reactant1-Bromo-3-tert-butylbenzeneHCID 343798—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
Product1-(3-Tert-butyl-phenyl)-4-methylene-cyclohexanolHCID 5973374381%

Reaction Steps

A solution of 1.7 M tert-butyllithium in pentane (32.0 mL, 54.4 mmol) was added to a solution of 1-bromo-3-tert-butyl-benzene (5.54 g, 26.0 mmol) in tetrahydrofuran (60 mL) at −78° C. After stirring for 1 h, cyclohexanone (2.00 g, 18.2 mmol) in tetrahydrofuran (15 mL) was added. After stirring for 18 h, during which time the solution warmed to ambient temperature, the solution was diluted with saturated aqueous ammonium chloride and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The residue was flash chromatographed with 49:1, 24:1, 23:2 hexanes:ethyl acetate as the eluant to yield 3.61 g (81% yield) of 1-(3-tert-butyl-phenyl)-4-methylene-cyclohexanol as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07385085B2
Source datasetuspto-grants-2008_06
ORD IDord-f0668dfcdcd04782a255a587cf61429e
Source noteuspto-grants-2008_06