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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454017Generated: November 1, 2026

Docosanoic Acid → HCID 24985706, compound

https://huagongshe.com/reaction/1454017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDocosanoic AcidHCID 8215—
ReactantAcetyl bromideHCID 10482—
ReactantN-(2-Hydroxyethyl)-N-methylguanidineHCID 83440—
ReactantCalcium ChlorideHCID 5284359—
SolventDichloromethaneHCID 6344—
ProductHCID 24985706HCID 24985706—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476749B1
Source datasetuspto-grants-2009_01
ORD IDord-e72c7c26c1444f85ab80bc243c0b89f3
Source noteuspto-grants-2009_01