HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(Trifluoromethyl)cyclohexane-1-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Iodoxybenzoic acid | HCID 108794 | — |
| Reactant | HCID 178520944 | HCID 178520944 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(Trifluoromethyl)cyclohexane-1-carbaldehyde | HCID 19763100 | 125.2% |
Reaction Steps
After dissolving [cis-4-(trifluoromethyl)cyclohexyl]methanol (2.04 g, 10.2 mmol) in dimethylsulfoxide (30 ml), 2-iodoxybenzoic acid (4.00 g, 14.3 mmol) was added thereto and stirred at room temperature overnight. Water and ethyl acetate were added to the reaction mixture, the insoluble matter was removed by filtration, and then the filtrate was separated into layers. The organic layer was washed with water and a saturated sodium chloride aqueous solution, dried over sodium sulfate, and concentrated to afford the title compound as a colorless oil (2.3 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09051333B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-e8e52f2b652e41d387388aa0b2345957 |
| Source note | uspto-grants-2015_06 |