HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 56631556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Docosanyl-p-toluenesulfonate | HCID 11145291 | — |
| Reactant | L-Cysteine, N-(1-oxohexadecyl)- | HCID 12151201 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 56631556 | HCID 56631556 | — |
Reaction Steps
4.8 g of docosanyl-p-toluenesulfonate and 5 g of potassium carbonate are added to 3.6 g of N-palmitoyl-(L)-cysteine in 50 ml of ethanol. The mixture is heated under stirring and in a nitrogen atmosphere at 80° for 20 hours. After evaporating to dryness the residue is acidified with 1 N HCl so as to obtain a pH of about 3 and then it is distributed between chloroform and water. After having dried and evaporated the chloroform layer a colourless crystalline residue is obtained, which is recrystallized from ethyl acetate. There is thus obtained the N-palmitoyl-S-docosanyl-(L)-cysteine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04439425 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-32474f89e7f5439ba93eeecf7509d264 |
| Source note | uspto-grants-1984_03 |