Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Hydroxy-2'-nitrobiphenyl | HCID 15541112 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2'-Nitrobiphenyl-4-yl sulfamate | HCID 9904187 | 71.8% |
Reaction Steps
108 mg of 2′-nitrobiphenyl-4-ol was dissolved in 1.5 ml of N,N-dimethyformamide, and a suspension of 120 mg of sodium hydride in 1.5 ml of N,N-dimethyformamide was added thereto under cooling with ice, followed by stirring for 10 minutes under cooling with ice. 367 mg of sulfamoyl chloride was added to this mixture, followed by stirring at room temperature for 3 hours. After water was added to the reaction mixture, the product was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium. sulfate. After the solvent was distilled off, the resulting crude product was purified by TLC (using a 1:1 mixture of ethyl acetate and hexane as the developing solvent) to obtain 106 mg of 2′-nitrobiphenyl-4-yl sulfamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06762205B1 |
|---|
| Source dataset | uspto-grants-2004_07 |
|---|
| ORD ID | ord-2e704ae4ed14478688fb927a2c15fb97 |
|---|
| Source note | uspto-grants-2004_07 |
|---|