HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydrosulfide → 2-Chloro-4-(ethylsulfonyl)benzenethiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Reactant | 2-Chloro-4-(ethylsulfonyl)-1-fluorobenzene | HCID 57904725 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Chloro-4-(ethylsulfonyl)benzenethiol | HCID 67390639 | — |
Reaction Steps
Sodium hydrosulphide (0.252 g) was added to the product from example 4 step (i) (11.0 g) in dry DMF (10 ml) and stirred at RT for 2 h. The mixture was diluted with 2M sodium hydroxide solution and extracted with diethylether. The aqueous layer was acidified with 2M hydrochloric acid, extracted with ethyl acetate, dried and evaporated under reduced pressure, crude yield 1.60 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022248B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-2c5ad7ee73c7461dbae0cf95dc3459cd |
| Source note | uspto-grants-2011_09 |