HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 1,3-Cyclohexadiene-1-carboxylic acid, 2,6,6-trimethyl-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl 2,6,6-trimethylcyclohexa-2,4-diene-1-carboxylate | HCID 118199 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 1,3-Cyclohexadiene-1-carboxylic acid, 2,6,6-trimethyl-, ethyl ester | HCID 118201 | — |
Reaction Steps
A mixture of 2.0 g of 2,6,6-trimethyl-1-ethoxycarbonyl-2,4-cylohexadiene [prepared according to the process indicated in Example 1], 100 mg of p-toluenesulphonic acid and 25 ml of anhydrous benzene were refluxed for 4 hours in a nitrogen atmosphere. The resulting solution was diluted with pentane, washed with a 5 % solution of sodium bicarbonate, then with water, and then dried over Na2SO4 and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028278 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-062c75b6511c45838ce5dacbd2b6898a |
| Source note | uspto-grants-1977_06 |