HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 54557924, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino2,4-hexadienoate | HCID 44325574 | — |
| Reactant | N-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate | HCID 86743575 | — |
| Product | HCID 54557924 | HCID 54557924 | — |
Reaction Steps
The procedure is as in Example 4 for the preparation of ethyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino-2,4-hexadienoate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (8 g), a 2M ethanolic solution of sodium ethylate (14 cc) and ethyl 1-(3-biphenylyl)acetate (6.7 g) in ethanol (30 cc). After purification by chromatography on a silica column with dichloromethane as eluent, diethyl 2-dimethylamino-5-(3-biphenylyl)-2,4-hexadienedioate (4.2 g) is obtained in the form of a yellow oil, and is used in the curde state in the subsequent syntheses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04886835 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-b1614d6b443c453bb3e0d50f38ad1fc0 |
| Source note | uspto-grants-1989_12 |