HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → Dimethyl ((4-hydroxyphenyl)methylene)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Dimethyl ((4-hydroxyphenyl)methylene)malonate | HCID 103565 | 96.4% |
Reaction Steps
To a mixture of 4-hydroxybenzaldehyde (280.9 g), dimethyl malonate (289.2 mL) and toluene (1.12 mL) were successively added acetic acid (13.2 mL) and piperidine (11.4 mL). After dehydration under refluxing at internal temperature of 70° C.–75° C. for about 4 hr, the mixture was cooled to internal temperature of not more than 10° C. and stirred further for 1 hr. The precipitated crystals were collected by filtration and washed with toluene (350 mL) to give the title compound (compound [8]; 523.7 g, yield 96.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06995271B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-97c3258f75f947e8a1e86821318edbec |
| Source note | uspto-grants-2006_02 |