HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-tert-Butyl-2-hydroxy-3-(trifluoromethyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-tert-Butyl-2-(trifluoromethyl)phenol | HCID 12652102 | — |
| Product | 5-tert-Butyl-2-hydroxy-3-(trifluoromethyl)benzaldehyde | HCID 19861817 | — |
Reaction Steps
0.1 mole of 2-trifluoromethyl-4-tert-butylphenol and 0.1 mole of hexamethylenetretramine is dissolved in trifluoroacetic acid (150 ml.) and the mixture refluxed for 8 hours. After this time, 150 ml. of water and 50 ml. of concentrated hydrochloric acid is added. This mixture is then refluxed for 1/2 hour. The reaction mixture is cooled and extracted with ether (5 × 50 ml.) and the ether extract is dried over magnesium sulfate. The ether is evaporated and the residue is crystallized from ethanol to yield 3-trifluoromethyl-5-t-butyl salicylaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04044153 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-b948bd4972e4478aa723e8a81a0856db |
| Source note | uspto-grants-1977_08 |