HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluorobenzyl bromide → HCID 22049898, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluorobenzyl bromide | HCID 68007 | — |
| Reactant | HCID 178516518 | HCID 178516518 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22049898 | HCID 22049898 | 37.7% |
Reaction Steps
According to Scheme 13 Step 1: The title compound was prepared from pyridine-2,4-diol (1 eq, 2.52 mmol, 0.28 g) and 1-(bromomethyl)-3-fluorobenzene (3 eq, 7.56 mmol, 0.93 mL) according to the procedure described for Example 1 Step 2. Reaction conditions: 17 h under reflux in DMF. The crude product was purified by flash chromatography on silica gel (CH2Cl2/AcOEt 90/10) to afford 1-(3-fluorobenzyl)-4-(3-fluorobenzyloxy)pyridin-2(1H)-one as a white solid (0.95 mmol, 0.29 g, 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399493B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-1d72061226544d9792b964495cde5380 |
| Source note | uspto-grants-2013_03 |