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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930212Generated: November 2, 2026

Piperidin-4-ol → 1-Cyclopropylpiperidin-4-ol

https://huagongshe.com/reaction/1930212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
Reactant(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product1-Cyclopropylpiperidin-4-olHCID 51582809—

Reaction Steps

5 g of 4-hydroxypiperidine were dissolved in methanol. 23.8 mL of 1[(1-ethoxycyclopropyl)oxy]trimethylsilane and 5.8 g of sodium cyano borohydride were added and the mixture was reacted at 60° C. for 12 h. The same amounts of the two reagents were added again and stirring was continued at 60° C. for another 12 h. The mixture was diluted with methanol, filtered over celite and evaporated to dryness. The residue was taken up in ethyl acetate, extracted twice with 2N sodium hydroxide and once with brine, dried over sodium sulfate and evaporated to dryness. The residue was purified by silica gel chromatography to yield 2 g of product 20, MS: 141 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188117B2
Source datasetuspto-grants-2012_05
ORD IDord-615de8dad020428a8303dff4ec524236
Source noteuspto-grants-2012_05