HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 70467484, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Veratraldehyde | HCID 8419 | — |
| Reactant | HCID 20222317 | HCID 20222317 | — |
| Product | HCID 70467484 | HCID 70467484 | 95.8% |
Reaction Steps
A solution of 8.4 g of 3,4-dimethoxybenzaldehyde, 11.4 g of 2-carboxymalonanilic acid, and 4.3 g of piperidine in 50 ml of benzene is heated under reflux for 3 hours with the removal of water as formed during the reaction period. After the completion of the reaction, the reaction mixture is cooled and the precipitated crystals are collected by filtration and dried to obtain 19.7 g of piperidinium N-(3,4-dimethoxycinnamoyl)anthranilate (95.8% yield), m.p. 154°-156° C. The compound structure is confirmed by elemental analysis, and by IR and NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04623724 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-6aeb4923f21648b2a38954da26d17e09 |
| Source note | uspto-grants-1986_11 |