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 ice-water, 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 | US04399163 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-7bd598844ca24a16b2192ad16cb2f5e0 |
| Source note | uspto-grants-1983_08 |