HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Phenylcyclohexane-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 22167780 | HCID 22167780 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Phenylcyclohexane-1-carbaldehyde | HCID 15535150 | 82.3% |
Reaction Steps
To a solution in tetrahydrofuran (10.0 mL) of the compound (3.59 g) obtained in step (1) above, 3 mol/L hydrochloric acid was added and the mixture was refluxed for 4 hours. After cooling the reaction mixture to room temperature, water was added to it and three extractions were conducted with ethyl acetate. The combined organic layers were washed with water and then concentrated under reduced pressure to give the titled compound as a colorless oil (2.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422240B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-38286e8de73d47358ac6c4445fc3cce7 |
| Source note | uspto-grants-2016_08 |