HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 2-[(Phenylsulfanyl)methyl]pentanedinitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4-Dicyano-1-butene | HCID 74080 | — |
| Product | 2-[(Phenylsulfanyl)methyl]pentanedinitrile | HCID 10059179 | — |
Reaction Steps
A mixture of thiophenol (3.63 g.), 2N aqueous sodium hydroxide (25 ml.) and 2-methyleneglutaronitrile (3.2 g.) was stirred at room temperature for 18 hours. The mixture was extracted with diethyl ether, and the ether extract washed with water and then dried and evaporated to dryness to give 2-(phenylthiomethyl)glutaronitrile which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670592 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-adf5cc9a29534517bcb85d14c634c86b |
| Source note | uspto-grants-1987_06 |