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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266005Generated: October 25, 2026

Dopamine → Dopamine ribonamide

https://huagongshe.com/reaction/1266005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDopamineHCID 681—
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
ReactantRibonolactoneHCID 111064—
SolventAcetoneHCID 180—
ProductDopamine ribonamideHCID 131723850188.1%

Reaction Steps

D-(+)-Ribonic acid gamma-lactone (2.0 gm, 13.5 mmol) was added to methanol (25 mL) in a 100 mL round bottom flask with stirring until dissolved, and then an additional 5 min. 3-Hydroxytyramine (2.6 gm, 13.5 mmol) was added slowly, allowing it to dissolve, with stirring, over the course of about 10 minutes. Triethylamine (1.4 gm, 13.5 mmol) was then added and the reaction mixture refluxed for 4 hr. in the dark, during which time the solution acquired a slight yellow color. Solvents were removed by rotary evaporation using anhydrous ethanol as an azeotrope to remove any residual water. The resultant dried product constituted a thick syrup which solidified upon standing (1 hr.) to give a white solid. The white solid product was stirred (1 hr.) with acetone (40 mL), again resulting in a white solid as a product. The resultant solid was collected by filtration and dried in vacuo for 6 hrs. yielding dopamine ribonamide (3.83 gm, 12.7 mmol, 94.1% yield .) 1H and 13C-NMR results and CHN analyses were consistent with structure. Melting point was 90-91° C. Predicted C13H19N1: (301.30): C, 51.82; H, 6.36; N, 4.65; Analysis results of synthesis product: C, 51.67; H, 6.40; N, 4.69.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548484B1
Source datasetuspto-grants-2003_04
ORD IDord-d32a9931e11640c1bfea3a351358a08d
Source noteuspto-grants-2003_04