HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Hydroxy-3,3-diphenylpropanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Hydroxy-3,3-diphenylpropanenitrile | HCID 266076 | — |
Reaction Steps
The solution of 8.2 g of acetonitrile in 200 ml of tetrahydrofuran is added dropwise to the solution of 14.08 g of butyl lithium in 125 ml of tetrahydrofuran and 125 ml of n-hexane while stirring at -70° under nitrogen and stirring is continued for 1 hour. Thereupon the solution of 36.4 g benzophenone in 200 ml o tetrahydrofuran is added dropwise and the mixture stirred for 20 minutes at room temperature. It is poured onto 300 g of ice and 100 ml of 3N hydrochloric acid, the organic layer separated and the aqueous phase extracted three times with 50 ml of diethyl ether. The combined organic solutions are dried, evaporated and the residue recrystallized from ethanol, to yield the β-hydroxy-β,β -diphenyl-propionitrile melting at 136°-138°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04042701 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-67107f62c72546acb1ef75204f6c1e78 |
| Source note | uspto-grants-1977_08 |