HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 3-(Benzyloxy)-2-methylpropanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methacrylonitrile | HCID 31368 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(Benzyloxy)-2-methylpropanenitrile | HCID 13531535 | — |
Reaction Steps
Benzyl alcohol (108 g.; 1 mole) was stirred and treated with 0.3 g. of 50% by weight sodium hydride in a mineral oil dispersion. To the resulting solution was added dropwise 415 ml. (335 g.; 5moles) of methacrylonitrile over a 40 minute period, at room temperature. The reaction mixture was heated at 60°-65° C. for 5 hours then cooled, acidified with 1 N aqueous H2SO4 and diluted with ether. The ether solution was washed twice with saturated brine then dried, filtered and concentrated in vacuo. Distillation of the residue gave, after removal of low boiling materials, 149.3 g. (85%) of rac. 3-benzyloxy-2-methylpropionitrile as a colorless liquid, b.p. 90°-93° C. (0.02 mm Hg.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04111961 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-fe82928b26de460dac9770d85f034bef |
| Source note | uspto-grants-1978_09 |