HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → HCID 178467228, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 13099799 | HCID 13099799 | — |
| Product | HCID 178467228 | HCID 178467228 | — |
Reaction Steps
Heterocyclic molecules are also derived from the above polyfunctional small molecules, which behave similarly. For example, 5-bromo-4,4-diethoxy-3-oxovaleronitrile is reacted with hydrazine, forming (via hydrazone formation, cyclization and ethanol elimination) 3-cyanomethyl-4-ethoxypyrazole; and acetimido 3-bromo-2,2-diethoxypropionate is cyclized on warming to produce 3-methyl-5-(2-bromo-1,1-diethoxyethyl)-1,2,5-oxadiazole. The latter is deketalized by warming in 95% formic acid to produce the corresponding 3-methyl-5-(2-bromoacetyl)-1,2,5-oxadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04443621 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-c5cc437779964b299c7f3e99497983bf |
| Source note | uspto-grants-1984_04 |