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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452022Generated: October 30, 2026

2-(2-(2-Azidoethoxy)ethoxy)ethanol → Mono-2-(2-(2-(4-(methylene)-1H-1,2,3-triazol-1-yl)ethoxy)ethoxy)ethanol-curcumin

https://huagongshe.com/reaction/452022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-(2-Azidoethoxy)ethoxy)ethanolHCID 11008438—
ReactantSodium AscorbateHCID 23667548—
ReactantMono-Propargyl CurcuminHCID 88539422—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Solventtert-ButanolHCID 6386—
ProductMono-2-(2-(2-(4-(methylene)-1H-1,2,3-triazol-1-yl)ethoxy)ethoxy)ethanol-curcuminHCID 13173071926%

Reaction Steps

To a stirred solution of Mono-Propargyl Curcumin 5 (63 mg, 0.16 mmol) and 2-(2-(2-azidoethoxy)ethoxy)ethanol (46 mg, 0.26 mmol) in tBuOH (1.1 mL) and CHCl3 (0.3 mL) was added a prepared solution of Cu(OAc)2 (8 mg, 0.03 mmol) and sodium ascorbate (13 mg, 0.07 mmol) in H2O (1.3 mL). After vigorous stirring overnight the solvent was removed under vacuum. The mixture was dissolved in CHCl3, washed with H2O and the organic phase was separated, dried over Na2SO4 and evaporated. Purification was performed by column chromatography, eluting with CH2Cl2-CH2Cl2: MeOH 98:2. Yield 26%. NMR NMR 1H (CDCl3), δ (ppm): 3.55-3.60 (m, 8H); 3.72-3.72 (t, 3H); 3.87-3.94 (m, 8H); 4.54-4.55 (t, 2H); 5.80 (s, 1H); 6.07 (s, 1H); 6.46-6.50 (dd, 2H); 6.92-6.94 (d, 1H); 7.05-7.12 (m, 5H); 7.56-7.60 (q, 2H); 7.92 (s, 1H).). MS (ESI) calcd. for C30H35N3O9: 581.61. Found: 582.3 [M+H]+, 604.3 [M++Na], 620.3 [M++K].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487139B2
Source datasetuspto-grants-2013_07
ORD IDord-b47b36a534c54e639febfd0283672cb1
Source noteuspto-grants-2013_07