HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Phenyl-3-phenylamino-benzo(b)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2-Phenyl-2-(phenylsulfanyl)acetic acid | HCID 239605 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Phenyl-3-phenylamino-benzo(b)thiophene | HCID 16640361 | — |
Reaction Steps
3.0 g of anilide of phenylthio-phenyl acetic acid (colourless needles in a mixture of benzene and petroleum ether mp 142°-143°) in 130 g of polyphosphoric acid are heated to 100° for 19 hours. The cooled reaction mixture is poured onto water, made alkaline by concentrated ammonia and extracted with methylene chloride. By drying over sodium sulphate and evaporating the extracts of methylene chloride, 1.7 g (60.0% of theory) of yellow oil are obtained which are recrystallized in ethanol: 1.5 g (45% of theory) of yellow crystals, mp 150°-151° (ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04157399 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-72aa0048b1f947589c78b839a1434659 |
| Source note | uspto-grants-1979_06 |