HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Bromide → N-(2-Bromoethyl)-N-[2-(4-cyanophenoxy)ethyl]methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Methanesulfonic acid 2-{[2-(4-cyanophenoxy)ethyl]methanesulfonylamino}ethyl ester | HCID 86616241 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(2-Bromoethyl)-N-[2-(4-cyanophenoxy)ethyl]methanesulfonamide | HCID 69075823 | — |
Reaction Steps
To a solution of methanesulfonic acid 2-{[2-(4-cyanophenoxy)ethyl]-methanesulfonylamino}ethyl ester (10 g, 0.028 mol; see step (iii) above) in dry acetone (100 mL), was added lithium bromide (4.8 g, 0.055 mol). The reaction mixture was added refluxed overnight under a nitrogen atmosphere, before being filtered and concentrated to give the title compound. Yield: 10 g (97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354917B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-34a6591cfe56468ba7e3757dc14c94c1 |
| Source note | uspto-grants-2008_04 |