HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2-Piperazin-1-ylethoxy)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-(2-Chloroethoxy)acetamide | HCID 11018931 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-Piperazin-1-ylethoxy)acetamide | HCID 21188362 | 39.5% |
Reaction Steps
A mixture of 13.15 g of (2-chloroethoxy)acetamide (0.1 mol) and 43 g of anhydrous piperazine (0.5 mol) in 250 ml of toluene is introduced into a round-bottomed flask fitted with a water-cooled condenser and a mechanical stirrer. The mixture is heated at the reflux temperature for 4 hours. The precipitate formed is filtered off while hot and the solvent of the filtrate is evaporated off under reduced pressure to dryness. The evaporation residue is purified by chromatography on silica gel (eluent: 14/5/1 (v/v/v) of dichloromethane/methanol/28% aqueous ammonia solution). 7.4 g of 2-[2-(1-piperazinyl)ethoxy]acetamide are obtained in the form of a yellow oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140501 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-52ae3c6cd0ef47f6959db87d2afc36c5 |
| Source note | uspto-grants-2000_10 |