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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454015Generated: November 1, 2026

Decanoic Acid → HCID 24985704, compound

https://huagongshe.com/reaction/1454015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDecanoic AcidHCID 2969—
ReactantAcetyl bromideHCID 10482—
ReactantN-(2-Hydroxyethyl)-N-methylguanidineHCID 83440—
ReactantCalcium ChlorideHCID 5284359—
SolventDichloromethaneHCID 6344—
ProductHCID 24985704HCID 24985704—

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 10.60 mL (125 mmol) of acetyl bromide and 25 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 9.64 mL (50 mmol) of Decanoic acid is added in one portion and the reaction is slowly heated to about 65° C. for about 6 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; 1/5) to yield pure 2-(1-methylguanidino)ethyl decanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476749B1
Source datasetuspto-grants-2009_01
ORD IDord-e1e3e7cd884a40c5bb724d9273961d38
Source noteuspto-grants-2009_01