HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Chloromethyl)-2,3-dihydro-1,4-benzodioxin → HCID 15541331, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Chloromethyl)-2,3-dihydro-1,4-benzodioxin | HCID 95320 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 1-(3-Nitrophenyl)piperazine | HCID 2760216 | — |
| Solvent | 2-Hexanone | HCID 11583 | — |
| Product | HCID 15541331 | HCID 15541331 | — |
Reaction Steps
A solution of 54.2 mmol (10 g) of 2-chloromethyl-2,3-dihydro-1,4-benzodioxin, 54.2 mmol (9.2 g) of 3-nitrophenylpiperazine and 6 g of potassium hydrogen carbonate in 100 ml of methyl-4-pentanone is heated at reflux for 72 hours. After cooling, the reaction mixture is concentrated. The residue is taken up in 200 ml of water and extracted with 200 ml of dichloromethane. The organic phase is dried over magnesium sulphate, concentrated and purified by chromatography on silica gel, using as eluant a 99/1/0.1 dichloromethane/methanol/ammonium hydroxide mixture, to yield the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026357B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-94fc9a147e76413cb18075da90909d92 |
| Source note | uspto-grants-2006_04 |