HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Butyl-4-hydroxy-3,5,5-trimethyl-2-cyclohexen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | 2,7,9,9-Tetramethyl-1,4-dioxaspiro[4,5]dec-6-en-8-one | HCID 13209183 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Butyl-4-hydroxy-3,5,5-trimethyl-2-cyclohexen-1-one | HCID 14759600 | — |
Reaction Steps
A solution of 20 g of 2,7,9,9-tetramethyl-1,4-dioxaspiro[4,5]dec-6-en-8-one (prepared by the method of Example III) in hexane is stirred while a solution of n-butyl lithium in hexane is added dropwise. When no additional exotherm occurs, the addition is stopped and the mixture is stirred for about 15 minutes. Water is added with stirring to hydrolyze the lithium salt. The organic layer is separated, and the hexane is allowed to evaporate leaving oily crystals which are recrystallized from cyclohexane yielding 10 g of 4-butyl-4-hydroxy-3,5,5-trimethyl-2-cyclohexyl-1-one, melting point 90°-93° C. The compound exhibits the following spectral characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04076854 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-620e2bca7dc74e1cb442123c18b08004 |
| Source note | uspto-grants-1978_02 |