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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724768Generated: October 25, 2026

Dicyclohexylcarbodiimide → 3-O-(4-dimethylaminobutanoyl)-1,2-O-dioleylglycerol

https://huagongshe.com/reaction/724768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2,3-Bis[(9Z)-9-octadecen-1-yloxy]-1-propanolHCID 5380343—
Reactant4-(Dimethylamino)butyric acid hydrochlorideHCID 12691640—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
Product3-O-(4-dimethylaminobutanoyl)-1,2-O-dioleylglycerolHCID 8675186087.1%

Reaction Steps

In 6 ml of methylene chloride-N,N-dimethylformamide (1:2) was dissolved 120 mg (0.20 mmol) of 1,2-O-dioleylglycerol, followed by addition of 168 mg (1 mmol) of 4-dimethylaminobutyric acid hydrochloride. Then, 206 mg (1 mmol) of N,N'-dicyclohexylcarbodiimide (DCC) and 25 mg (0.2 mmol) of 4-dimethylaminopyridine were further added and the reaction was conducted at ambient temperature overnight. The precipitated byproduct urea was filtered off using a glass filter and the filtrate was concentrated to dryness under reduced pressure and treated with methylene chloride-saturated aqueous sodium hydrogen carbonate solution. After phase separation, the methylene chloride layer was dried over sodium sulfate and the solvent was distilled off under reduced pressure. The residue was subjected to column chromatography (silica gel/methylene chloride-methanol) to provide 123 mg (87%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705188
Source datasetuspto-grants-1998_01
ORD IDord-67c0825cd6a54a299578d974dc75d89a
Source noteuspto-grants-1998_01