HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylhydroquinone → HCID 54443355, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylhydroquinone | HCID 16043 | — |
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | 4-Oxazolin-2-one | HCID 186114 | — |
| Reactant | 2-Ethenyl-4,4-dimethyl-1,3-oxazol-5(4H)-one | HCID 9812794 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54443355 | HCID 54443355 | — |
Reaction Steps
A solution of 100 g. of N,N-dimethylethylenediamine in 40 cc. of benzene was added dropwise to a stirring solution of 16.4 g. of 2-vinyl-4,4-dimethyl-5-oxazolone in 50 cc. of benzene. The oxazolone solution contained a few milligrams of t-butylhydroquinone as a polymerization inhibitor. An external water bath was used to maintain the resultant solution at about 25° C. The solution was stirred about 2 hours, filtered through Celite, and evaporated. The residue after evaporation was triturated with hexane and the mixture filtered to provide N-(N',N'-dimethyl-β-aminoethyl)-2-methyl-2-acrylamidopropanoic acid amide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04424272 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-f684a47319c144afa7e7365e4b62a48c |
| Source note | uspto-grants-1984_01 |