HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-(2-bromophenyl)acetate → Methyl(2-cyanophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-(2-bromophenyl)acetate | HCID 8063364 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Catalyst | Iron chloride (FeCl3) | HCID 24380 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl(2-cyanophenyl)acetate | HCID 1512623 | — |
Reaction Steps
To a stirring solution of copper (I) cyanide (1.2 eq) in dimethylformamide (2.1 M) at room temperature was added slowly a solution of 2a in dimethylformamide (8.7 M). The reaction was heated to reflux overnight then cooled to room temperature. A solution of iron (III) chloride (1.2 eq) in H2O (0.3 M) was added slowly to the vigorously stirred solution. The resulting solution was extracted with ethyl acetate (3×). The organic phases were combined then washed with brine (1×), dried over sodium sulfate, filtered, concentrated in vacuo and purified by flash chromatography (15% ethyl acetate/hexanes) to afford the product as a clear oil. (70%) 1H NMR (300 MHz, CDCl3) δ 6.09 (m, 1H), 5.98 (m, 1H), 5.79 (m, 2H), 2.29 (s, 2H), 2.11 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06992193B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-5aa1c99be26a4bbd8d1b0b7de2924d43 |
| Source note | uspto-grants-2006_01 |