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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12638Generated: October 25, 2026

Water → 4-[Dimethylaminomethyl]-cyclohexane-carbaldehyde

https://huagongshe.com/reaction/12638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
Reactant4-[(Dimethylamino)methyl]cyclohexan-1-oneHCID 23337803—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product4-[Dimethylaminomethyl]-cyclohexane-carbaldehydeHCID 86627886—

Reaction Conditions

Temperature0 °C

Reaction Steps

(Methoxymethyl)triphenylphosphonium chloride (25.7 g, 75 mmole) was suspended in absolute THF (100 ml) under argon, potassium tert-butylate (8.42 g, 75 mmole) dissolved in absolute THF (70 ml) was added dropwise, and then stirred for 15 minutes at 0° C. The corresponding 4-[dimethylaminomethyl]-cyclohexanone 8 (50 mmole), dissolved in absolute THF (75 ml), was then added dropwise to the above solution and stirred overnight at RT. The mixture was hydrolysed by adding dropwise water (38 ml) and 6N HCL 112 ml) while cooling with iced water. After stirring for one hour at RT the mixture was extracted with ether (10×50 ml), the aqueous phase was adjusted to pH 11 with 5N NaOH, shaken with ethyl acetate (3×50 ml), dried over Na2SO4, and concentrated by evaporation in vacuo. The crude product was purified by flash chromatography with ethyl acetate/cyclohexane (1:1). As a rule two diastereomers were obtained in different ratios.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728028B2
Source datasetuspto-grants-2010_06
ORD IDord-bc612dc3b5e34a4491165424b9751861
Source noteuspto-grants-2010_06