HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cesium carbonate → 4-Methoxybenzyl (3-bromophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | (3-Bromophenyl)acetic acid | HCID 74653 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Methoxybenzyl (3-bromophenyl)acetate | HCID 86619553 | — |
Reaction Steps
A DMF (30 mL) solution of (3-bromophenyl)acetic acid (2.5 g, 11.6 mmol), cesium carbonate (3.78 g, 11.6 mmol) and 4-methoxybenzyl chloride (1.82 g, 11.6 mmol) was stirred overnight at room temperature. The solution was then partitioned between ethyl acetate and water. The organic phase was washed with water (3×), brine and dried over magnesium sulfate. The solution was filtered, concentrated and the residue purified by silica gel chromatography using a hexanes/ethyl acetate gradient to give the title compound. 1H NMR (400 MHz, CDCl3): δ 7.43-7.39 (m, 2H); 7.29-7.24 (m, 2H); 7.20-7.16 (m, 2H); 6.90-6.86 (m, 2H); 5.07 (s, 2H); 3.81 (s, 3H); 3.60 (s, 2H). LCMS1 3.70 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318760B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-df83517b623849eaaa1a7849219003e3 |
| Source note | uspto-grants-2012_11 |