HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2-(4-bromo-3,5-dimethylphenoxy)ethyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(4-Bromo-3,5-dimethylphenoxy)ethanamine | HCID 22688749 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-(4-bromo-3,5-dimethylphenoxy)ethyl)methanesulfonamide | HCID 86697208 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a cooled (0° C.) solution of 2-(4-bromo-3,5-dimethylphenoxy)ethanamine (100 mg) and triethylamine (63 μL) in dichloromethane (2 mL) is added methanesulfonyl chloride (32 μL). The mixture is stirred for 2 hours at 0° C. Then the mixture is partitioned between dichloromethane and water. The organic phase is separated, washed with brine and dried (MgSO4). The solvent is evaporated and the residue is purified by HPLC on reversed phase to give the title compound. Yield: 90 mg; LC (method 7): tR=1.01 min; Mass spectrum (ESI+): m/z=322 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642585B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-5bdcf8c67df74aa5851c07702d842fbb |
| Source note | uspto-grants-2014_02 |