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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612373Generated: November 1, 2026

Water → (3-Methylpiperidin-3-yl)methanol

https://huagongshe.com/reaction/612373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantEthyl nipecotateHCID 98969—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(3-Methylpiperidin-3-yl)methanolHCID 19594566—

Reaction Conditions

Temperature-5 °C

Reaction Steps

To ethyl nipecotate (1.3 g) in THF (20 mL) at r.t was added potassium bis(trimethylsilyl)amide (18 mL of a 0.5 M solution in toluene). After 1 h, methyl iodide (0.5 mL) was added and the mixture was stirred for 15 h. Water was added and the mixture extracted with ether. The organics were washed with brine, dried and concentrated. The residual material (1.3 g) was dissolved in THF (20 mL) and treated with lithium aluminum hydride (8.7 mL of a 1 M solution in THF) at r.t. After 15 h, the mixture was cooled to -5° C. and aqueous sodium potassium tartrate was added followed by concentrated NH4OH, 10 N NaOH and the resulting mixture was stirred for 30 min. The mixture was filtered through anhydrous sodium sulfate and the filtrate was concentrated from toluene twice. The residual oil (1 g), containing the title compound, was used without further purification in Step 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06004950
Source datasetuspto-grants-1999_12
ORD IDord-fd4781567fb1477c8a384b27f708f0ee
Source noteuspto-grants-1999_12