HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl phenylacetate → Diethyl 2-dimethylamino-5-phenyl-2,4-hexadienedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl phenylacetate | HCID 7590 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | N-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate | HCID 86743575 | — |
| Reactant | Diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate | HCID 86743580 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl 2-dimethylamino-5-phenyl-2,4-hexadienedioate | HCID 53828842 | — |
Reaction Steps
The procedure is as in Example 2 for the preparation of diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (10 g), a 2M ethanolic solution of sodium ethylate (21 cc) and ethyl phenylacetate (5.6 cc) in ethanol (100 cc). After purification by chromatography on a silica column, with a mixture of cyclohexane and ethyl acetate (80:20 by volume) as eluent, diethyl 2-dimethylamino-5-phenyl-2,4-hexadienedioate (4.6 g) is obtained, and is used in the crude state in the subsequent phases.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04971979 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-64fe82719b364240a99203da96053b9b |
| Source note | uspto-grants-1990_11 |