HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-t-Butyl-1,3,4-thiadiazol-5-yl Isocyanate → 2-[1-Allyl-3-(5-t-butyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-t-Butyl-1,3,4-thiadiazol-5-yl Isocyanate | HCID 6452456 | — |
| Reactant | 2-Allylaminoacetaldehyde | HCID 20548476 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[1-Allyl-3-(5-t-butyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde | HCID 20324643 | — |
Reaction Steps
A mixture of 5-t-butyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.05 mole), the dimethyl acetal of 2-allylaminoacetaldehyde (0.1 mole) and benzene (60 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and reflux condenser. The reaction mixture is heated at reflux for a period of about 15 minutes. After this time the mixture is stripped of benzene under reduced pressure to yield a solid product as the residue. The residue is then recrystallized to yield the desired product the dimethyl acetal of 2-[1-allyl-3-(5-t-butyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04018787 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-898accb450e543c3a55147bcc9576849 |
| Source note | uspto-grants-1977_04 |