HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N6-(1-Oxohexadecyl)-L-lysine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Palmitic Acid | HCID 985 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Lysine monohydrochloride | HCID 69568 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | N6-(1-Oxohexadecyl)-L-lysine | HCID 100425 | 73% |
Reaction Steps
Following the procedure of A. Paquet Can. J. Chem. 54, 733 (1976), 353 mg. (1 mmol) of the succinimidylester of hexadecanoic acid, prepared as in example 2, was suspended in 2 ml acetone and added to a solution of 183 mg (1 mmol) L-lysine hydrochloride and 0.27 ml (ca. 2 mmol) triethylamine in 2 ml water. The reaction mixture was stirred vigorously for at least 4 h, then neutralized with acetic acid and diluted with water. The precipitate was removed by filtration and washed with water, methanol and ether. Repeated crystallizations from acetic acid/water and acetic acid gave 280 mg (73%) colourless crystals, m.p. 240°-245° C. (reported 210°-220° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05047535 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-412eac3935a74c7f8adb0d2fa1c6d42c |
| Source note | uspto-grants-1991_09 |