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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 20510553 | HCID 20510553 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20510601 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04371644 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-25c7c46092184de58c380fc181596439 |
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| Source note | uspto-grants-1983_02 |
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