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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448185Generated: October 26, 2026

Tyramine → N-Caffeoyltyramine

https://huagongshe.com/reaction/448185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTyramineHCID 5610—
ReactantTriethylamineHCID 8471—
ReactantCaffeic AcidHCID 689043—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-CaffeoyltyramineHCID 9994897—

Reaction Steps

A solution of caffeic acid (300 mg; 1.66 mmol) and of triethylamine (1.5 eq; 2.49 mmol) in DMF (3.5 mL) is cooled to 4° C. using an ice bath. An amine, tyramine (1 eq; 1.66 mmol) is added to the medium, followed by addition of a solution of BOP (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; 1 eq; 1.66 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 is obtained in the form of a white precipitate after purification by chromatography on a column of silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481593B2
Source datasetuspto-grants-2013_07
ORD IDord-e34b3c9ae2fa4e769410f7134ab8ed04
Source noteuspto-grants-2013_07