HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 4-[4-(Trifluoromethoxy)phenoxy]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 68485568 | HCID 68485568 | — |
| Solvent | Isobutanol | HCID 6560 | — |
| Product | 4-[4-(Trifluoromethoxy)phenoxy]piperidine | HCID 16115439 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Potassium hydroxide (10.7 g) was heated to 100° C., and dissolved in isobutanol (15 mL). An isobutanol (25 mL) solution of 1-ethoxycarbonyl-4-(4-trifluoromethoxyphenoxy)piperidine (12.03 g) was dropwise added thereto while noticing generation of carbon dioxide gas. After the dropwise addition, the mixture was heated and stirred at 100° C. for 2 hours; then the solvent was concentrated; and toluene (40 mL) was added to the obtained residue. The toluene solution was washed with water (40 mL×2), and then the solvent was concentrated under reduced pressure to obtain a target compound as a light orange solid substance. The yield amount was 5.73 g (98% based on trifluoromethoxyphenol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552188B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-89ef3452cdf54d6d86e0b914fa936344 |
| Source note | uspto-grants-2013_10 |