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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196067Generated: October 26, 2026

Triethylamine → N-docosahexaenoyl-D-serine

https://huagongshe.com/reaction/1196067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantD-SerineHCID 71077—
ReactantDocosahexenoic acidHCID 175542—
Reactant4-Hydroxyphenyldimethylsulfomethyl sulfateHCID 86745786—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductN-docosahexaenoyl-D-serineHCID 5400113640.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-hydroxyphenyldimethylsulfomethyl sulfate (trade name: SANCELER-DSP, manufactured by Sanshin Kagaku Kogyo Co., Ltd.) 2.66 g (0.01 mol) was heated and dissolved in 40 ml of acetonitrile. Docosahexaenoic acid 3.28 g (0.01 mol) was added to the solution obtained in a stream of nitrogen, and stirred at 0° C. To the mixture solution, dicyclohexyl carbodiimide 2.06 g (0.01 mol) was added little by little, and the solution was stirred for 2 hours at 0° C. and then for 2 hours at room temperature. The solution reacted was filtered to remove dicyclohexyl urea, and the filtrate was distilled in vacuo to obtain oily residue. D-serine 1.05 g (0.01 mol) and triethyl amine 1.4 ml (0.01 mol) were added to 10 ml of water. An acetonitrile solution of the above oily residue was added to the mixture with stirring, and stirred for 10 hours at room temperature. After reaction, the reaction mixture was concentrated under reduced pressure. The concentrate was adjusted to pH 2 or 3 with 6N-HCl, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous sodium acetate, and freed of solvent in vacuo. The oily residue obtained was purified by column chromatography (column: 2.5×15 cm) on 50 g of silica gel and N-docosahexaenoyl-D-serine 1.7 g was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112863
Source datasetuspto-grants-1992_05
ORD IDord-87da6933365e4652bb43e0f4147837d5
Source noteuspto-grants-1992_05