HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethanol → 1-(2-Hydroxyethyl)-4-methylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-(2-Hydroxyethyl)-4-methylpiperazine | HCID 231184 | 75% |
Reaction Steps
N-methyl-piperazine (10 g, 100 mmoles) and 2-chloroethanol (8.5 g,100 mmoles) are stirred at 100° C. for 4 hours. 250 ml of acetone are added to the very viscous reaction mixture and the resulting suspension is neutralised with 15 ml of triethylamine. After filtration of the triethylammonium chloride, the solvent is evaporated under reduced pressure. The desired compound is obtained after purification by chromatography on an alumina column (eluent:ethyl acetate) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06040328 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-e537cb58ace447138073678f86b273cb |
| Source note | uspto-grants-2000_03 |