HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-(2-Chloroethyl)-1,4-dimethyl-2-piperazinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(2-Hydroxyethyl)-1,4-dimethyl-2-piperazinone | HCID 13376739 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-Chloroethyl)-1,4-dimethyl-2-piperazinone | HCID 13376741 | — |
Reaction Steps
Thionyl chloride (1.5 mL) was added dropwise to an ice cooled methylene chloride (5 mL) solution of 3-(2-hydroxyethyl)-1,4-dimethyl-2-piperazinone (0.40 g, described in Example 1). The reaction mixture was stirred for 30 min and poured on an ice solution of 10% sodium bicarbonate. The mixture was extracted with methylene chloride, and the organic extract was dried and evaporated to give the title compound: IR (CHCl3) 1635 cm-1 ; and NMR (CDCl3) δ 2.35 (s, 3H) and 2.90 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04482714 |
| Source dataset | uspto-grants-1984_11 |
| ORD ID | ord-99aeb12ef8364fc3beb4d1e190749932 |
| Source note | uspto-grants-1984_11 |