HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 14631589, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2-ethylphenol | HCID 87877 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14631589 | HCID 14631589 | 569.5% |
Reaction Steps
Potassium carbonate (21.6 g, 0.16 mol) followed by benzyl bromide (6.2 mL, 52 mmol) were added to a solution of 4-bromo-2-ethyl-phenol (1.6 g, 7.9 mmol, from step 1 of Example B(98)) in DMF (75 mL). The mixture was stirred for 20 hours and then partitioned between 1N HCl and EtOAc. The organic layers were washed with brine, dried over Na2SO4 and concentrated. The crude yellow oil was purified by flash column chromatography (hexanes) to give the desired product (13.1 g, 87%). 1H NMR (400 MHz, CDCl3): δ 1.20 (t, J=7.6 Hz, 3 H), 2.56 (q, J=7.8 Hz, 2 H), 5.13 (s, 2 H), 6.84 (d, J=8.3 Hz, 1 H), 7.04 (dd, J=8.3, 2.3 Hz, 1 H), 7.32 (m, 1 H), 7.38 (m, 3 H), 7.47 (d, J=7.9 Hz, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148226B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-3b51f4a0e3f54fd9bb3be0813e147a4a |
| Source note | uspto-grants-2006_12 |