HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → N,N-dimethyl-2-(phenylthio)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 2-(Phenylthio)benzoic acid | HCID 15210 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(Phenylsulfanyl)benzoyl chloride | HCID 291322 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N,N-dimethyl-2-(phenylthio)benzamide | HCID 21402688 | — |
Reaction Steps
Following the procedure described in Example 1, 2-(phenylthio)benzoyl chloride is prepared from 0.065 mole of 2-(phenylthio)benzoic acid and excess thionyl chloride. A solution of the oily acid chloride in 50 ml. of benzene is added dropwise with stirring to a solution of 7 g. of dimethylamine in 50 ml. of benzene. The mixture is heated briefly to refluxing. Evaporation of the solvent under reduced pressure leaves N,N-dimethyl-2-(phenylthio)benzamide as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04018830 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-52c36e262bb74d0babc4acd9d434083a |
| Source note | uspto-grants-1977_04 |