HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 20320706, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Ethylparaben | HCID 8434 | — |
| Reactant | ((2-Bromoethyl)thio)benzene | HCID 78553 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 20320706 | HCID 20320706 | — |
Reaction Steps
This compound was prepared by the condensation procedure 1A. The required intermediate 2-bromoethylphenyl sulphide may be prepared by condensing 1,2-bromoethane and thiophenol in sodium hydroxide solution, in a manner analogous to that used for preparation of the intermediates for compounds of Example Nos. 62-73, but a method which gives better yields uses the scheme: ##STR25## Condensation with ethyl 4-hydroxybenzoate gave 1-(4-ethoxycarbonylphenoxy)-2-phenylthio ethane, m.p. 50°-51° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04098816 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-196aa8b03e024a0396e9eac2f4f4ebcf |
| Source note | uspto-grants-1978_07 |