HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,4-Pentanedione, 3-(p-hydroxybenzyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | 4-(Chloromethyl)phenol | HCID 35684 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Pentanedione, 3-(p-hydroxybenzyl)- | HCID 203886 | 78% |
Reaction Steps
A solution of p-chloromethyl phenol in acetonitrile (Example 12) was reacted with equimolar dimethyl amine and equimolar 2,4-pentanedione by stirring together for one hour. The reactive mixture was diluted with water, acidified with hydrochloric acid, extracted with ether, and then the ether extract was dried with sodium sulfate. The residual oil was triturated with benzene to yield 78% of 3(4' hydroxybenzyl)-2,4-pentanedione, M.P. 93°-94.5°C. Infrared and nuclear magnetic resonance spectra confirmed the identity of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983178 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-4793b7491f9244c88d5ba45693ad5c40 |
| Source note | uspto-grants-1976_09 |