HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-t-Butyl-1,3,4-thiadiazol-5-yl Isocyanate → 3-[1-Methyl(5-t-butyl-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-t-Butyl-1,3,4-thiadiazol-5-yl Isocyanate | HCID 6452456 | — |
| Reactant | 3-(Methylamino)propanal | HCID 21254778 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-[1-Methyl(5-t-butyl-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde | HCID 21400098 | — |
Reaction Steps
A mixture of 5-t-buty-1,3,4-thiadiazol-2-yl isocyanate dimer (6 grams), the dimethyl acetal of 3-methylaminopropionaldehyde (4.0 grams) and benzene (50 ml) are charged into a glass reaction flask equipped with a mechanical stirrer and reflux condenser. The reaction mixture is heated at reflux, with stirring, for a period of about 5 minutes. After this time the reaction mixture is stripped of benzene to yield a residue. The residue is then recrystallized to yield the desired product the dimethyl acetal of 3-[1-methyl-(5-t-butyl-1,3,4-thiadiazol-2-yl)ureido]propionaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04006009 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-3a0552192fd944958ccc5608e0f17b7f |
| Source note | uspto-grants-1977_02 |