HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetoacetate → HCID 53744655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178419636 | HCID 178419636 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53744655 | HCID 53744655 | — |
Reaction Steps
A solution of p-phenoxyphenylmagnesium bromide (obtained from 2.49 g. of 4-bromodiphenyl ether and 0.24 g. of magnesium in 100 ml. of ether) is added dropwise at 20°, with stirring, to a solution of 1.3 g. of acetoacetic acid ethyl ester in 40 ml. of ether, and the mixture is stirred for a further two hours, the resulting alcoholate is decomposed by means of ice and saturated NH4Cl solution, and the ethereal phase is dried and evaporated to give 3-p-phenoxyphenyl-3-hydroxybutyric acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049823 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-8214920da2ff4daaafe92c12701ec5b4 |
| Source note | uspto-grants-1977_09 |