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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329026Generated: October 26, 2026

Sodium Hydroxide → 2-((1-Benzylpiperidin-4-yl)oxy)ethanol

https://huagongshe.com/reaction/329026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant8-Benzyl-1,4-dioxa-8-azaspiro[4.5]decaneHCID 726449—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-((1-Benzylpiperidin-4-yl)oxy)ethanolHCID 2029534767%

Reaction Steps

106.8 g of (0.8 mole) of aluminum chloride were added to a 2 liter, 3-neck flask and then 800 ml of anhydrous ether were added thereto with strong cooling. The mixture was stirred for 30 minutes and then a suspension of 7.6 g (0.2 mole) of lithium aluminum hydride in 200 ml of ether was added thereto. The mixture was stirred for 30 minutes and then a solution of 93.2 g (0.4 mole) of 8-benzyl-1,4-dioxa-8-aza-spiro [4,5] decane in 400 ml of anhydrous ether was added thereto dropwise. After the addition, stirring was continued at room temperature for 2 hours and 1 liter of water was then slowly added with strong cooling. The mixture was made alkaline with 90 g of sodium hydroxide pellets and the ether phase was decanted off. The aqueous layer was extracted again with ether and the combined ether phases were dried and the ether removed by distillation. The residue was distilled to obtain 63 g (67% yield) of 2-[1-benzyl-4-piperidyloxy]-ethanol in the form of a clear oil boiling at 140° C at 0.1 mm Hg and having a refractive index nD20 = 1.633.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04018922
Source datasetuspto-grants-1977_04
ORD IDord-eff47d7de94a413385251666cee7d8b0
Source noteuspto-grants-1977_04