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 (8.7 grams), the diethyl acetal of 2-allylaminoacetaldehyde (8.0 grams) and benzene (50 ml) was charged into a glass reaction flask equipped with a mechanical stirrer and thermometer. The reaction mixture was then warmed with stirring until the reactants dissolved. After this time the reaction mixture was stripped of benzene to yield an oil. This oil was dissolved in an ether-pentane mixture and was treated with diatomaceous earth and filtered. The filtrate was then stripped of solvent to yield the desired product the diethyl acetal of 2-[1-allyl-3-(5-t-butyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde as a dark red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028375 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-472293e49f084c759e4e949c2fa80ab3 |
| Source note | uspto-grants-1977_06 |