HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → Benzaldehyde 4-methyl-2-(5-t-butyl-1,3,4-thiadiazol-2-yl)semicarbazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | Benzaldehyde 5-t-butyl-1,3,4-thiadiazolyl hydrazone | HCID 70487433 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzaldehyde 4-methyl-2-(5-t-butyl-1,3,4-thiadiazol-2-yl)semicarbazone | HCID 53934083 | 22.1% |
Reaction Steps
Methyl isocyanate (1.88 g) was added to a stirred suspension of benzaldehyde 5-t-butyl-1,3,4-thiadiazolyl hydrazone (7.8 g) in ethyl acetate (60 ml). Triethylamine (3 drops) was then added and the mixture was stirred for 2 hours. The solvent was evaporated to give a white solid, purified by chromatography. The pure fractions were combined and recrystallised from a mixture of ethyl acetate and hexane to give benzaldehyde 4-methyl-2-(5-t-butyl-1,3,4-thiadiazol-2-yl)semicarbazone (2.1 g, 22%) as a white powder, mp 115°-116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04501605 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-35ad602451fe48829f4634441d5927f9 |
| Source note | uspto-grants-1985_02 |