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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448184Generated: October 30, 2026

Dopamine → N-Feruloyl dopamine, trans-

https://huagongshe.com/reaction/448184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDopamineHCID 681—
ReactantTriethylamineHCID 8471—
ReactantFerulic AcidHCID 445858—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-Feruloyl dopamine, trans-HCID 16119330—

Reaction Steps

A solution of ferulic acid (300 mg; 1.54 mmol) and of triethylamine (1.5 eq; 2.31 mmol) in DMF (3.5 mL) is cooled to 3 or 4° C. using an ice bath. An amine, 3-hydroxytyramine (dopamine) (1 eq; 1.54 mmol) is added to the medium, followed by addition of a solution of BOP (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; (1 eq; 1.54 mmol) in dichloromethane (3.5 mL); the mixture is stirred for about thirty minutes in the ice bath and then for 20 hours at room temperature. Stirring is then stopped and the dichloromethane is evaporated off under vacuum. 30 mL of water are added to the remaining solution and the mixture obtained is extracted with ethyl acetate (3×75 mL). The organic phase is successively washed with 100 mL of 1N HCl solution, 100 mL of water and 100 mL of 1M sodium bicarbonate (NaHCO3) solution. It is then dried over sodium sulfate and evaporated to dryness. The product obtained is in the form of a white precipitate after chromatography on a column of silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481593B2
Source datasetuspto-grants-2013_07
ORD IDord-38f65c87bccb4fbcb5b491bbd4d0c3b1
Source noteuspto-grants-2013_07