HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (3-Benzyloxy-4-nitrophenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (Phenylthio)acetonitrile | HCID 78891 | — |
| Reactant | Benzyl-2-nitrophenyl Ether | HCID 57359178 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (3-Benzyloxy-4-nitrophenyl)acetonitrile | HCID 13629306 | — |
Reaction Steps
To a suspension of NaOH (68.44 g 1.71 mol, Aldrich, 20-40 mesh beads) in 171 mL of DMSO a solution of benzyl-2-nitrophenyl ether (39.23 g, 0.171 mol) and (phenylthio)acetonitrile (25.54 g, 0.171 mol, Lancaster) in 171 mL of DMSO was added dropwise for 10 min and stirred at r.t. for another 25 min. A mixture of 430 g of ice and 430 g of conc. HCl was added. The product precipitated and crystallized. The reaction mixture was cooled down in a refrigerator and filtered. The precipitate was dried on air (hood!) and recrystallized from EtOAc-hexanes. Yield 32.03 g (70%), mp 78-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596734B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-07042c1f284e4e9f9227e21fb80c0ce4 |
| Source note | uspto-grants-2003_07 |