HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfite → Sodium 2-(4-bromo-phenyl)-ethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(4-Bromophenyl)ethanol | HCID 72851 | — |
| Reactant | 4-Bromophenethyl Methanesulfonate | HCID 14485090 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | Sodium 2-(4-bromo-phenyl)-ethanesulfonate | HCID 57751107 | — |
Reaction Steps
Methanesulfonic acid 2-(4-bromo-phenyl)-ethyl ester (1.39 g) prepared from 2-(4-bromo-phenyl)-ethanol and methanesulfonyl chloride, and Na2SO3 (816 mg) were reacted in ethanol/water (1/1), to obtain a crude product of 2-(4-bromo-phenyl)-ethanesulfonic acid sodium salt as a colorless plate-like crystal. Then, thionyl chloride (3 ml) was left to react in the presence of DMF (500 μl), to obtain 2-(4-bromo-phenyl)-ethanesulfonyl chloride, and further N-methylpiperazine (73 μl) was left to react in dichloromethane (2 ml) in the presence of triethylamine (54 μl), to obtain 1-[2-(4-bromo-phenyl)-ethanesulfonyl]-4-methyl-piperazine as a yellow solid (94 mg, 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022205B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-c70ee80a402f422985b6a054a8fe19e3 |
| Source note | uspto-grants-2011_09 |