HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 2-(3-Phenoxyphenyl)propanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | alpha-(Methylthio)-alpha-(m-phenoxyphenyl)propionitrile | HCID 54570589 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3-Phenoxyphenyl)propanenitrile | HCID 118006 | 84.5% |
Reaction Steps
451 mg of alpha-(methylthio)-alpha-(m-phenoxyphenyl)propionitrile was dissolved in 1 ml of anhydrous methanol, and 1.1 ml of a 2.3 M methanol solution of sodium methanethiolate was added. The mixture was stirred at room temperature for 2 hours. An aqueous solution of ammonium chloride (2 g/10 ml) was added, and the mixture was extracted with 10 ml of ether three times. The extract was washed with 15 ml of water three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel; hexane and methylene chloride) to afford 316 mg (yield 83%) of alpha-(m-phenoxyphenyl)-propionitrile as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04340740 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-8967a194c26d489bb2a33a8c55e08eee |
| Source note | uspto-grants-1982_07 |