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 | 3-Allyl-4,5-dimethoxy-benzaldehyde | HCID 3144059 | — |
| Reactant | di-(2-ethylhexyl) malonate | HCID 9923500 | — |
| 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 mole), of di-(2-ethylhexyl) malonate (16.4 g, 0.05 mole), of toluene (20 ml), of acetic acid (0.41 ml) and of piperidine (0.77 ml) was heated at reflux for 5 hours with a Dean Stark. After cooling, washing the toluene phase with water, drying and evaporating off the solvent, an orange-colored oil was obtained, which was 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 (colorless oil, 15 g, yield=64%) which had the following characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05053290 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-b01eeb22940641c59449f81f3156f927 |
| Source note | uspto-grants-1991_10 |