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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(2-(2-Azidoethoxy)ethoxy)ethanol | HCID 11008438 | — |
| Reactant | Sodium Ascorbate | HCID 23667548 | — |
| Reactant | Mono-Propargyl Curcumin | HCID 88539422 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Mono-2-(2-(2-(4-(methylene)-1H-1,2,3-triazol-1-yl)ethoxy)ethoxy)ethanol-curcumin | HCID 131730719 | 26% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447023B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-79f55600219c4c2a8d67961975ee03d9 |
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| Source note | uspto-grants-2016_09 |
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