HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 2-(Phenylthio)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-(Phenylthio)benzoic acid | HCID 15210 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(Phenylsulfanyl)benzoyl chloride | HCID 291322 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(Phenylthio)benzamide | HCID 2728632 | — |
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 acetone is added dropwise with stirring to 100 ml. of concentrated ammonium hydroxide. The mixture is heated to refluxing for 3 hours. On cooling, the product separates and is collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04018830 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-e580e373a9c049d899d63a59ebe8faa9 |
| Source note | uspto-grants-1977_04 |