HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malic Acid → HCID 86737303, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malic Acid | HCID 525 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-carbobenzyloxy-4-(4,14-pentadecadienylamino)benzoyl chloride | HCID 54048902 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86737303 | HCID 86737303 | — |
Reaction Steps
To a warm solution of N-carbobenzyloxy-4-(4,14-pentadecadienylamino)benzoyl chloride and 1.3 g. triethylamine in 100 ml. ether is treated with 2 g. malic acid. An immediate precipitate forms, but the mixture is refluxed for one hour and filtered while hot. The solid is wahsed several times with hot ether, then the ether is evaporated to yield a white solid. The product is dissolved in tetrahydrofuran (100 ml.) and hydrogenated over 600 mg. 10% palladium-on-carbon at 50 psi until hydrogen uptake stops. The catalyst is filtered. The solution is evaporated and the residue is crystallized from acetic acid to yield the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04230878 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-d91652d05d774f8589b8d58ae0ae05d6 |
| Source note | uspto-grants-1980_10 |