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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758192Generated: October 31, 2026

2-Methyl-2-butanol → HCID 20510601, compound

https://huagongshe.com/reaction/1758192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-butanolHCID 6405—
ReactantButyl bromideHCID 8002—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 20510553HCID 20510553—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
ProductHCID 20510601HCID 20510601—

Reaction Steps

To 300 ml of t-pentyl alcohol were added potassium t-pentoxide (prepared from 5.0 g of metallic potassium) and 6.6 g of 2,2-bis{4-[2-hydroxy-3-(4-hydroxy-2,2,6,6-tetramethylpiperidino)propoxy]-phenyl}propane (obtained as described in Example 1); the mixture was refluxed for 2 hours. The reaction mixture was cooled to ambient temperature and there were added 10.0 g of n-butyl bromide. The mixture was heated at 50°-60° C. for 15 hours. After completion of the reaction, the reaction mixture was condensed by evaporation under reduced pressure and the residue was extracted with benzene. The extract was washed with water and dried over anhydrous potassium carbonate. The solvent was removed from the dried solution by evaporation under reduced pressure and the resulting residue was purified by column chromatography through silica gel eluted with a 2:5 by volume mixture of ethyl acetate and benzene. The desired Compound No. 30 was obtained in the form of a colourless viscous oil having an Rf value of 0.68 on thin-layer chromatography on silica gel developed with a 8:1:1:1 by volume mixture of ethyl acetate, benzene, ethanol and triethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371644
Source datasetuspto-grants-1983_02
ORD IDord-25c7c46092184de58c380fc181596439
Source noteuspto-grants-1983_02