HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 66958832, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Hydrazine, ethyl-, ethanedioate (1:1) | HCID 96181 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 66958840 | HCID 66958840 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66958832 | HCID 66958832 | — |
Reaction Steps
A modification of the method described in Part A of Example 11 was followed. A solution of ethyl 2,4-dioxo-6-phthalimidohexanoate, sodium salt (37.64 g, 0.110 mol) in glacial acetic acid (160 L) was cooled to 10° C. before the addition of ethylhydrazine oxalate (16.52 g, 0.110 mol). During the addition, the reaction temperature was maintained between 9 and 11° C. The reaction was complete in two hours. The crude product, a reddish-orange oil, was treated with diethyl ether (150 mL) to form a solid, which was isolated by filtration to provide 26.5 g of ethyl 1-ethyl-5-(2-phthalimidoethyl)-1H-pyrazole-3-carboxylate as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879849B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-1023664235cb4040838288a1b733b488 |
| Source note | uspto-grants-2011_02 |