HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 3,3-Diacetyl-propionic acid-benzylester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Product | 3,3-Diacetyl-propionic acid-benzylester | HCID 54450814 | 51% |
Reaction Steps
10 grams acetylacetone were reacted with 5 grams of a 50% suspension of sodium hydride in paraffin oil and with 25 grams bromoacetic acid-benzylester in accordance with a procedure analogous to that set out in Example (2b). 3,3-diacetyl-propionic acid-benzylester having a Kp0.005 of 126°-128° C. was obtained. This substance was further reacted with phenylhydrazine by a procedure analogous to that set out in Example (2c). 3,5-dimethyl-1-phenyl-pyrazol-4-acetic acid-benzylester, having a Kp0.001 of 205°-209° C., was obtained in a yield of 51%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04146721 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-dbd05169129b4b61b6f790bfc49f5b7f |
| Source note | uspto-grants-1979_03 |