HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malonic Acid → 3-(4-Heptylphenyl)prop-2-enoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Heptylbenzaldehyde | HCID 10921634 | — |
| Reactant | p-n-Heptylcinnamic acid | HCID 53734772 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(4-Heptylphenyl)prop-2-enoyl chloride | HCID 54198035 | — |
Reaction Steps
8.8 G. of p-n-heptylbenzaldehyde and 8.74 g. of malonic acid are dissolved in 7 ml. of absolute pyridine, treated with 8 drops of piperidine and heated at 90°-100° C. for 68 hours. The mixture is then taken up in ether and washed with dilute hydrochloric acid. After recrystallization from ether/hexane, there are obtained 7.5 g. of p-n-heptylcinnamic acid having a melting point of 121°-122° C. and a clearing point of 150°-153° C. 8.2 G. of this acid are boiled at reflux in 120 ml. of thionyl chloride for 30 minutes. The excess thionyl chloride is removed by distillation, the residue taken up three times in absolute toluene, concentrated and dried. The p-n-heptylcinnamic acid chloride obtained can be used in the process directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061587 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-5f90ec3a2e5b4aa7b1e6ba6e6613cfcf |
| Source note | uspto-grants-1977_12 |