HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 2-tert-Butylcyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium dichromate dihydrate | HCID 108005 | — |
| Reactant | 1-Tert-butylcyclohexan-1-ol | HCID 287917 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-tert-Butylcyclohexanone | HCID 102681 | — |
Reaction Steps
A solution of 31.25 g. (0.20 mole) t-butylcyclohexanol in 80 ml. of ethyl ether was cooled to 10° C. To this was added dropwise, with stirring, a solution of 21.0 g. (0.07 mole) sodium dichromate dihydrate and 15.75 ml. (0.30 mole) concentrated sulfuric acid in 100 ml. water while maintaining the reaction mixture below 25° C. The mixture was then warmed to room temperature, stirred for two hours, poured onto icewater, ether layer separated, the aqueous phase extracted again with ether and the combined extracts washed with water, sodium bicarbonate and dried (MgSO4). Evaporation of the ether afforded 30.6 g. (99%) of the desired ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04804782 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-10d3ff42868e44eaa6bc5acf6474c583 |
| Source note | uspto-grants-1989_02 |