HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Ethyl 2-(1H-1,2,3-triazol-1-YL)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178418936 | HCID 178418936 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-(1H-1,2,3-triazol-1-YL)acetate | HCID 10103365 | — |
Reaction Steps
129.2 g (5.6 mmol) of sodium are added slowly to 4.0 litres of ethanol. 400.0 g (5.6 mol) of 1,2,3-1H-triazole are then added, and 623 ml (938.2 g, 5.6 mol) of ethyl bromoacetate are added dropwise at an internal temperature of 20-25° C. The mixture is stirred at RT for 48 h. The precipitated solid is filtered off, the ethanol is removed under reduced pressure and the mixture is filtered again. The residue is taken up in ethyl acetate, filtered, again concentrated under reduced pressure and purified by distillation on a 30 cm column. The product is obtained at a bath temperature of 140° C., a head temperature of 60-115° C. and a pressure of 1 mbar. Yield: 440.0 g (50% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08067407B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-951eeb148d06444b83c2c93ba618087f |
| Source note | uspto-grants-2011_11 |