HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-(2-Bromo-phenylsulfanyl)-3-sulfino-benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromobenzenethiol | HCID 80598 | — |
| Reactant | 5-Carboxy-2-fluorobenzenesulfinic acid | HCID 10679678 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Bromo-phenylsulfanyl)-3-sulfino-benzoic Acid | HCID 22139410 | — |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
2-Bromobenzenethiol (25 g, 132 mmol) was added to a solution of 4-fluoro-3-sulfino-benzoic acid (13.5 g, 66 mmol) and NaOH pellets (11 g, 264 mmol) in water (30 ml). The yellow mixture was then degassed for 10 minutes and then heated to 140° C. for 48 hours. The reaction was then cooled to 0° C. and acidified to pH 4–5 (pH paper) with concentrated HCl. The precipitate formed was filtered, washed with hexane and was dried in a vacuum dessicator over activated silica overnight (20.69 g, 84%). m/z (LC-MS, ESP), RT=3.67 min, (M−−1)=373.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07049313B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-270abed976bf46dbb74feeddd5a3d306 |
| Source note | uspto-grants-2006_05 |