HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → HCID 13470300, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 13412-12-9 | HCID 5702622 | — |
| Reactant | HCID 20268352 | HCID 20268352 | — |
| Reactant | HCID 178483601 | HCID 178483601 | — |
| Product | HCID 13470300 | HCID 13470300 | — |
| Product | HCID 20268355 | HCID 20268355 | — |
Reaction Steps
Using a procedure similar to that described in Example 1, 0.5 mole of methyl 3-methylaminocrotonate and 0.5 mole of 3-[2-(2chlorophenoxy)-ethoxy]-benzoyl chloride are converted to methyl 3-methylamino-2-[3-(2-(2-chlorophenoxy)-ethoxy)-benzoyl]-crotonate of melting point 131°-133° C., the yield being 58%. When reacted with hydrazine hydrate by a procedure similar to that described in Example 1, this ester gives 5-methyl-4-methoxycarbonyl-3-[3-(2-(2-chlorophenoxy)-ethoxy)-phenyl]-pyrazole of melting point 127°-129° C., the yield being 59%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04537617 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-19d7ddf95a2d452a915f6742670b5bd3 |
| Source note | uspto-grants-1985_08 |