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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756844Generated: October 28, 2026

Dimethyl Sulfoxide → 4-(2,3-Epoxypropoxy)-1-octyloxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/1756844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantEpichlorohydrinHCID 7835—
ReactantSodium hydrideHCID 24758—
Reactant1-Octyloxy-2,2,6,6-tetramethylpiperidin-4-olHCID 11346683—
SolventTetrahydrofuranHCID 8028—
Product4-(2,3-Epoxypropoxy)-1-octyloxy-2,2,6,6-tetramethylpiperidineHCID 5398673016.3%

Reaction Steps

A mixture of 20.0 grams (70 mmol) of 4-hydroxy-1-octyloxy-2,2,6,6-tetramethylpiperidine (prepared in Example 5), 1.68 gram (70 mmol) of sodium hydride, 2 ml of dimethyl sulfoxide, and 150 ml of tetrahydrofuran is heated at reflux for three hours. The reaction mixture is cooled to room temperature, and a solution of 6.5 grams (70 mmol) of epichlorohydrin in 50 ml of tetrahydrofuran is added over a 5-minute period. The reaction mixture is stirred sixteen hours at room temperature and then partitioned between ether and water. The aqueous layer is extracted with ether and the combined ether solutions are dried over anhydrous magnesium sulfate before concentrating to yield an oil. Purification by flash chromatography (4:1 hexane:ethyl acetate) affords 3.9 grams (16% yield) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05442071
Source datasetuspto-grants-1995_08
ORD IDord-1737b3b5423943a791c33bfeb05623c3
Source noteuspto-grants-1995_08