HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 71515486, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 71547769 | HCID 71547769 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 71515486 | HCID 71515486 | 51.2% |
Reaction Steps
To a solution of (2,6-difluoro-3-hydroxyphenyl)(quinoxalin-6-yl)methanone (57 mg, 0.2 mmol, 1.0 eq.) in CH3CN (10 mL) were added K2CO3 (56 mg, 0.4 mmol, 2 eq.) and (bromomethyl)benzene (38 mg, 0.22 mmol, 1.1 eq). The resulting mixture was stirred at rt overnight, then concentrated. The residue was purified via flash column chromatography (PE/EA=10/1, v/v) to afford (3-(benzyloxy)-2,6-difluorophenyl)(quinoxalin-6-yl)methanone as brown solid (38.4 mg, 51.2%). LRMS (M+H+) m/z calculated 377.1, found 377.1. 1H NMR (CDCl3, 400 MHz) δ 8.93-8.95 (d, 2 H), 8.48 (s, 1 H), 8.39-8.41 (d, 1 H), 8.23-8.26 (d, 1 H), 7.33-7.45 (m, 5 H), 7.10-7.16 (m, 1 H), 6.91-6.95 (t, 1 H), 5.17 (s, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249111B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-c884d6dec16540eeb67c8d1f7188c059 |
| Source note | uspto-grants-2016_02 |