HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 19937045, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | di-(2-ethylhexyl) malonate | HCID 9923500 | — |
| Reactant | HCID 11217997 | HCID 11217997 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 19937045 | HCID 19937045 | 64% |
Reaction Steps
A mixture of 3™allyl-4,5-dimethoxybenzaldehyde (10.3 g, 0.05 moles), di-(2-ethylhexyl) malonate (16.4 g, 0.05 moles), toluene (20 ml), acetic acid (0.41 ml) and piperidine (0.77 ml) is heated to reflux using a Dean Stark. After cooling, washing the toluene phase with water, drying and evaporation of the solvent, an orange-coloured oil is obtained, which is purified by chromatography on a column of silica 60 (eluent: 90:10 heptane/ethyl acetate) to give di-(2-ethylhexyl) 3-allyl-4,5-dimethoxybenzalmalonate (colourless oil, 15 g, yield=64%), which has the following characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05175340 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-d725a560384140638fb515d85c326714 |
| Source note | uspto-grants-1992_12 |