Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Reactant | 1-(4-Bromophenyl)ethanol | HCID 95352 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 89581270 | HCID 89581270 | 94% |
Reaction Steps
NaH (300 mg, 60%, 7.5 mmol) was suspended in N,N-dimethylformamide. 1-(4-bromophenyl)ethanol was added to the above mixture and stirred at 40° C. for 0.5 hour. Then 2-chloropyrimidine was added to the above mixture and stirred at 100° C. for 12 hours. The mixture was concentrated to give a residue. The residue was purified by column chromatography (silica gel, petroleum ethe/ethyl acetate=3:1) to give 2-(1-(4-bromophenyl)ethoxy)pyrimidine as a white solid (2.6 g, 94%). LRMS (M+H+) m/z: calcd 278.01. found 278.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09206128B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-3d04a0fa34bf4256a176ada2470fb7c0 |
|---|
| Source note | uspto-grants-2015_12 |
|---|