HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propyl mercaptan → 4-Thiophen-2-ylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propyl mercaptan | HCID 7848 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | 2-(4-methoxyphenyl)thiophene | HCID 2769425 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Thiophen-2-ylphenol | HCID 3564197 | — |
Reaction Steps
To a solution of 8.80 g (2-(4-methoxyphenyl)thiophene (prepared from 2-thienylmagnesium bromide and p-iodoanisole) and 5.4 ml propanethiol in 100 ml dry dimethylformamide was carefully added 7.00 g 35% potassium hydride in mineral oil. The reaction mixture was heated at reflux under nitrogen for 16 hours. Isolation of the resulting product afforded after crystallization 2.42 g 4-(2-thienyl)phenol as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04857539 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-6af8107c215442038e8a7b4dff66d74b |
| Source note | uspto-grants-1989_08 |