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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067112Generated: October 31, 2026

Diisopropylamine → HCID 21196457, compound

https://huagongshe.com/reaction/1067112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantCyclohexanoneHCID 7967—
Reactant3-Methoxy-2-methylbenzaldehydeHCID 13162663—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21196457HCID 2119645775%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of diisopropylamine (1.44 ml) in THF (8 ml) was added n-BuLi (1.56M solution in hexane, 70 ml) at −60° C. The mixture was warmed to 0° C., stirred for 10 minutes, and recooled to −60° C. To the mixture was added cyclohexanone (0.98 g) in THF (5 ml). After stirring for 1 hour, 3-methoxy-2-methylbenzaldehyde (1.5 g) was added and the mixture was stirred for 1.5 hours at the same temperature. The reaction mixture was quenched with saturated NH4Cl solution, warmed to room temperature, extracted with EtOAc. The organic layer was washed with water and brine, dried over magnesium sulfate, evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane-EtOAc 4:1 to 2:1) to give 2-[hydroxy-(3-methoxy-2-methylphenyl)methyl]cyclohexanone (1.86 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245790B1
Source datasetuspto-grants-2001_06
ORD IDord-ee14f09175ef4242b56282fb4d29844e
Source noteuspto-grants-2001_06