HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 21520097, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium benzenethiolate | HCID 4110039 | — |
| Reactant | HCID 21520114 | HCID 21520114 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21520097 | HCID 21520097 | — |
Reaction Steps
A mixture of ethyl 3-butylthio-4-chloro-5-sulfamylbenzoate (0.85 g), thiophenol (0.6 ml), and dry ethanol (25 ml) containing 5 millimoles of sodium thiophenolate is refluxed for 6 hours. After evaporation in vacuo 1 N sodium hydroxide (20 ml) and ethanol (10 ml) are added, and the mixture is refluxed for 15 minutes. After cooling and extraction with diethyl ether, 3-butylthio-4-phenylthio-5-sulfamylbenzoic acid is precipitated from the aqueous layer by addition of 4 N hydrochloric acid. The precipitate is collected by filtration and recrystallized from aqueous ethanol to yield the desired acid having a melting point of 192° - 193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03950376 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-3b34266dddde4dae94d3429b4190b240 |
| Source note | uspto-grants-1976_04 |