HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → HCID 19833860, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Cyclohexanecarboxylic acid, 2,2-dimethyl-6-methylene- | HCID 12308779 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 19833860 | HCID 19833860 | 92.3% |
Reaction Steps
In a flask maintained under nitrogen and equipped with a mechanical stirrer, a suspension of K2CO3 (29.5 g, 0.241 mole) in an acetone (200 ml) solution of 2,2-dimethyl-6-methylene-1-cyclohexanecarboxylic acid (30.0 g, 0.179 ml) and ethyl bromide (23.3 g, 0.214 mole) was warmed up to reflux. After 2 h 30, the temperature was allowed to cool to 25° and the reaction mixture was poured on 5% NaOH, extracted with ether (twice), washed with H2O and sat. NaCl, dried over Na2SO4, filtered and the solvents evaporated. Distillation of the crude product yielded, at 90°/5.3×102Pa, 32.3 g of the desired ester (yield: 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05015625 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-a2d251936f8643f788c9b8364ac3a1f0 |
| Source note | uspto-grants-1991_05 |