HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzaldehyde → Ethyl 4,4,4-trichloro-2-(3-nitrophenylmethylene)-3-oxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Hexanoic Acid | HCID 8892 | — |
| Reactant | Ethyl 4,4,4-trichloro-3-oxobutyrate | HCID 77294 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 4,4,4-trichloro-2-(3-nitrophenylmethylene)-3-oxobutanoate | HCID 54196727 | 28.9% |
Reaction Steps
3-Nitrobenzaldehyde (7.55 g, 50 mmoles), ethyl 4,4,4-trichloro-3-oxobutanoate (18.33 g, 59.5 mmoles), piperidine (0.66 ml) and hexanoic acid (0.33 ml) were heated at reflux in toluene (130 ml) for 48 hours using a Dean and Stark apparatus. The mixture was cooled, evaporated to dryness in vacuo and crystallised by trituration with ethyl acetate/petroleum ether (60°-80°). Recrystallisation from 2-propanol gave the sub-title compound (5.3 g) mp 105.5°-7°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04607041 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-0f5d9b338d8f460eab0a9a6edb5f6d22 |
| Source note | uspto-grants-1986_08 |