HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (5-Bromo-6-chloro-pyridin-2-yl)-(4-chloro-benzyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (4-Chloro-benzyl)-(6-chloro-pyridin-2-yl)-amine | HCID 57619237 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (5-Bromo-6-chloro-pyridin-2-yl)-(4-chloro-benzyl)-amine | HCID 57619309 | — |
Reaction Steps
To (4-chloro-benzyl)-(6-chloro-pyridin-2-yl)-amine (538, 4.00 g, 0.0158 mol) in acetonitrile (66.7 mL, 1.28 mol) under an atmosphere of nitrogen, N-bromosuccinimide (2.81 g, 0.0158 mol) in acetonitrile (20 mL) was added slowly. The reaction was stirred at room temperature overnight, then poured into water and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, concentrated and crystallized with ethyl acetate in hexane to give a white solid (539, 2.60 g, 95.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722702B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-413fa884ba5e4bb9964bbac6cc4e12ba |
| Source note | uspto-grants-2014_05 |