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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 8-Benzyl-1,4-dioxa-8-azaspiro[4.5]decane | HCID 726449 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-((1-Benzylpiperidin-4-yl)oxy)ethanol | HCID 20295347 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04018922 |
|---|
| Source dataset | uspto-grants-1977_04 |
|---|
| ORD ID | ord-eff47d7de94a413385251666cee7d8b0 |
|---|
| Source note | uspto-grants-1977_04 |
|---|