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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075856Generated: November 1, 2026

2,2,6,6-Tetramethylpiperidine → HCID 21541288, compound

https://huagongshe.com/reaction/1075856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant1,2-Epoxy-3-[3-(2-pyridylmethyl)phenoxy]propaneHCID 12919852—
Solvent1-PentanolHCID 6276—
ProductHCID 21541288HCID 2154128818.9%

Reaction Steps

8.9 g of 2,2,6,6-tetramethylpiperidine is added to a solution of 15.0 g of 1,2-epoxy- 3-[3-(2-pyridylmethyl)phenoxy]propane in 45 ml of n-amyl alcohol, and the resulting mixture is heated on a water bath for 2 hours. The solvent is then removed, 200 ml of benzene is added to the residue, and the insoluble matter is filtered off with activated charcoal. The filtrate is washed with water, and extracted with two 100 ml portions of 5% hydrochloric acid. The aqueous layer is made alkaline with sodium hydroxide, and the separated oil is extracted with benzene. The benzene layer is washed with water, dried over anhydrous potassium carbonate, and the solvent is removed. The residual oil is purified by distillation to give 4.5 g of 1-(2,2,6,6-tetramethylpiperidino)-3-[3-(2-pyridylmethyl)phenoxy]-2 -propanol, boiling at 230°-235°C/0.15 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954776
Source datasetuspto-grants-1976_05
ORD IDord-1d651a62c6cf480d841d1c8aabbbff79
Source noteuspto-grants-1976_05