HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Fluorophenoxy)benzenesulphonyl chloride → 4-(4-Fluorophenoxy)benzene-1-thiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Fluorophenoxy)benzenesulphonyl chloride | HCID 2782757 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Fluorophenoxy)benzene-1-thiol | HCID 21705585 | 100% |
Reaction Steps
Lithium aluminum hydride (9.95 grams, 0.26 mole) was added in portions to a stirred solution of 4-(4-fluorophenoxy)benzenesulfonylchloride (30 grams, 0.105 mole) in tetrahydrofuran (700 mL). The resulting mixture was heated at reflux for 1.5 hours, cooled in an ice bath and quenched by addition of 10% aqueous sulfuric acid solution (100 mL). After stirring for 30 minutes, the mixture was filtered through Celite™ and the tetrahydrofuran was removed under vacuum. The residue was diluted with water and extracted with diethyl ether. The organic layer was washed with water and brine, dried over magnesium sulfate and concentrated under vacuum to provide the title compound as a white solid (23 grams, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06110964 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-349d59eb47f4417e8157bb11153bff4a |
| Source note | uspto-grants-2000_08 |