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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62588Generated: October 27, 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/62588

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 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 numberUS09447023B2
Source datasetuspto-grants-2016_09
ORD IDord-79f55600219c4c2a8d67961975ee03d9
Source noteuspto-grants-2016_09