HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → 5'-Fluoro-2'-Formyl-4-Methylthiobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4'-Chloro-5-fluoro-[1,1'-biphenyl]-2-carbaldehyde | HCID 19361943 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5'-Fluoro-2'-Formyl-4-Methylthiobiphenyl | HCID 19361946 | — |
Reaction Steps
85% potassium hydroxide solution (66 g) is dissolved in ethanol (700 ml) and cooled to room temperature. To this with stirring is added methyl mercaptan subsurface (50 g), water (2ml) and a solution of 4-chloro-5'-fluoro-2'-formylbiphenyl (234.5 g) in ethanol (300 ml). A slow stream of methyl mercaptan is continuously fed in while the reaction mixture is held at reflux for 3 hours. The reaction is poured into water (1 liter), and the solid is filtered off. The solid is recrystallized from benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020379 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-4aae6ecab7d04d8499cbb449b5ad94c5 |
| Source note | uspto-grants-2000_02 |