HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malic Acid → O-(4-hexadecylamino-2-thiophenecarbonyl)malic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malic Acid | HCID 525 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-[N-(carbobenzyloxy)-N-hexadecylamino]-2-thiophenecarbonyl chloride | HCID 20503621 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | O-(4-hexadecylamino-2-thiophenecarbonyl)malic acid | HCID 86738856 | — |
Reaction Steps
A warm solution of 4-[N-(carbobenzyloxy)-N-(hexadecyl)amino]-2-thiophenecarbonyl chloride and 1.3 g. of 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 washed 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, and the solution is evaporated. The residue is crystallized from acetic acid to yield the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382143 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-dd278f15741c4545b496cd60e1156566 |
| Source note | uspto-grants-1983_05 |