HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (3-Bromo-2,5-dimethoxy-phenyl)-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1-Bromo-3-chloromethyl-2,5-dimethoxy-benzene | HCID 10308154 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (3-Bromo-2,5-dimethoxy-phenyl)-acetonitrile | HCID 10149238 | 77% |
Reaction Steps
A solution of 1-Bromo-3-chloromethyl-2,5-dimethoxy-benzene 53 (7.0 g, 26.4 mmol) and KCN (1.7 g, 26.4 mmol) in DMSO (50 ml) was heated to 75° C. After 2 hr, the reaction was cooled and poured into water. The aqueous layer was extracted with EtOAc and the organic layer was dried and concentrated. The product was purified by column chromatography on silica gel (20% EtOac/Hex) to give 54 as an oil (5.2 g, 77%): 1H NMR (DMSO-d6) δ 7.20 (d, 1 H, J=3.0 Hz), 6.99 (d, 1 H, J=3.0 Hz), 4.00 (s, 2 H), 3.75 (s, 6 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022733B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-84fb0e07d5124db592d3d493673caede |
| Source note | uspto-grants-2006_04 |