Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Docosanoic Acid | HCID 8215 | — |
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | N-(2-Hydroxyethyl)-N-methylguanidine | HCID 83440 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 24985706 | HCID 24985706 | — |
Reaction Steps
In a dry 3-necked round bottomed flask, containing a magnetic stirrer, equipped with a dropping funnel, a reflux condenser protected from moisture by a calcium chloride filled drying tube and a rubber septum. The dropping funnel is filled with 12.73 mL (150 mmol) of acetyl bromide and 35 mL of dry DCM. The flask is charged with 35.14 g (300 mmol) of Creatinol and 150 mL of dry DCM, and cooled with an ice-water bath to about 0° C., under a nitrogen atmosphere. The acetyl bromide solution is then added slowly with stirring, over a period of 10 minutes, to the Creatinol solution. The solution is stirred for another 15 minutes, after which 23.84 g (70 mmol) of Docosanoic acid is added in one portion and the reaction is slowly heated to about 65° C. for about 12 hours. Then the solution is allowed to cool to room temperature, after which the solvent is removed under reduced pressure to yield the crude ester. The crude ester is then purified by flash chromatography (ethyl acetate/hexanes; 1/3) to yield pure 2-(1-methylguanidino)ethyl docosanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476749B1 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-e72c7c26c1444f85ab80bc243c0b89f3 |
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| Source note | uspto-grants-2009_01 |
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