HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 2-[1-Allyl-3-(5-t-butyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 2-t-Butyl-1,3,4-thiadiazol-5-yl Isocyanate | HCID 6452456 | — |
| Reactant | 2-Allylaminoacetaldehyde | HCID 20548476 | — |
| Solvent | Diethylether pentane | HCID 21877078 | — |
| 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 acetate of 2-allylaminoacetaldehyde (8.0 grams) and benzene (30 ml) was charged into a glass reaction flask equipped with a mechanical stirrer and reflux condenser. The reaction mixture was heated with stirring for a period of about 15 minutes. After this time the reaction mixture was stripped of benzene to yield an oil. The oil was dissolved in a diethyl ether-pentane mixture and was filtered through diatomaceous earth. The filtrate was 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 oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03958975 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-6c35f5b9c69f4a1491357d0ba19cf10d |
| Source note | uspto-grants-1976_05 |