HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → 1-(1,4-Benzodioxan-5-yl)-4-cyanomethylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Eltoprazine | HCID 65853 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-(1,4-Benzodioxan-5-yl)-4-cyanomethylpiperazine | HCID 10611289 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A solution of 1-(1,4-benzodioxan-5-yl)piperazin (11 g) and triethylamine (7 ml) in N-methyl-2-pyrrolidinone was treated dropwise with chloroacetonitrile (4.5 g). After stirring for 2 h at 100° C. the mixture was poured onto ice and extracted with ethyl acetate. The organic phase was washed with water, dried over magnesium sulfate, filtered, and concentrated in vacuo. The product, 1-(1,4-benzodioxan-5-yl)-4-cyanomethylpiperazine, was obtained as an oil (17.4 g) which was sufficiently pure for use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753661 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-eeb312d2a22e48b48f084c41e02aa3f8 |
| Source note | uspto-grants-1998_05 |