HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanal → HCID 178450112, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | HCID 178424185 | HCID 178424185 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 178450112 | HCID 178450112 | 91.5% |
Reaction Steps
A mixture of 133 parts tolyltriazole, 79.3 parts n-butyraldehyde, 100.1 parts cyclohexanol and 1.3 parts paratoluene sulphonic acid is heated in 600 parts cyclohexane with simultaneous azeotropic removal of the water formed during the reaction. The reaction is complete after 2 hours. Upon cooling to ambient temperature, the reaction mixture is washed with dilute sodium carbonate solution, then with water and finally dried over anhydrous magnesium sulphate. The dried reaction mixture is filtered and evaporated under reduced pressure and then stripped under vacuum (100° C./4 Pa) to yield 262.9 parts (91.5 %) of 1-(1-cyclohexyloxybutyl) tolyltriazole as a yellow oil. The product is distilled at 175° C./8 Pa to yield a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05032300 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-e8da9f9c78c54ccc9da7f9ce487e6f5e |
| Source note | uspto-grants-1991_07 |