HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Bromo-2-methoxy-5-(trifluoromethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methoxy-5-(trifluoromethyl)pyridine | HCID 2775312 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Bromo-2-methoxy-5-(trifluoromethyl)pyridine | HCID 14837018 | 34.7% |
Reaction Steps
To a stirred solution of 2-methoxy 5-(trifluoromethyl) pyridine (4 g, 22.58 mmol) was dissolved in acetonitrile (50 ml) was added NBS (6 g, 33.87 mmol) portion wise at 0° C. The reaction mixture was stirred for overnight at RT. The solvent was removed under vacuum, quenched with water (100 mL) and extracted with ethyl acetate. The combined organic layer was washed with water, brine, dried over sodium sulfate, and concentrated at reduced pressure to yield 3-bromo-2-methoxy-5-(trifluoromethyl)pyridine (12) as a pale yellow liquid (2 g, 34.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09163020B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-f8f8aec63b0142a99d32b4aa9a984ed3 |
| Source note | uspto-grants-2015_10 |