HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Diethyl 2-[[4-(methylthio)phenyl]methylene]propanedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 4-(Methylthio)benzaldehyde | HCID 76985 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Water | HCID 962 | — |
| Product | Diethyl 2-[[4-(methylthio)phenyl]methylene]propanedioate | HCID 13221107 | — |
Reaction Steps
4-(Methylthio)Benzaldehyde (3.04 g, .02 mol), diethyl malonate (3.20 g. .02 mol), toluene (25 mL), piperidine (4 drops) and acetic acid (2 drops) are mixed and heated at reflux for 2 hours with the water formed being removed azeotropically. The solution is cooled and 25 mL of water added stirring. After separation of the layers, the toluene is evaporated from the organic layer to yield the product, diethyl 2-[[4-(methylthio)phenyl]methylene]propanedioate, in essentially quantitative yield. When dissolved in methylene chloride, the product has an absorption maximum (λmax) at 330 nm in the ultraviolet absorption spectrum. The identity of the product is confirmed by mass spectroscopy analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04845188 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-77b5d0c0f78b4a40a24f9e1c86dcdda1 |
| Source note | uspto-grants-1989_07 |