HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-(4-chloro-2-hydroxymethylphenylthio)-N-methyl-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-2-(hydroxymethyl)thiophenol | HCID 13312619 | — |
| Reactant | 5-fluoro-N-methyl-2-nitroaniline | HCID 22905774 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-chloro-2-hydroxymethylphenylthio)-N-methyl-2-nitroaniline | HCID 23363142 | 87.1% |
Reaction Steps
The solution of 4-chloro-2-(hydroxymethyl)thiophenol (1.0 g) from Example 16, 5-fluoro-N-methyl-2-nitroaniline (1.0 g) and K2CO3 (0.81 g) in DMF (20 ml) was heated at 90° C. for 15 minutes. After leaving the solution to stand at room temperature, water was added to the solution prior to extraction in ethyl acetate. The organic layer was washed with saturated sodium chloride solution, and dried over anhydrous sodium sulfate. After removal of the solvent under reduced pressure, the residue was purified by chromatography on a silica gel column (methylene chloride) to give the title compound (1.62 g; 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05587392 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-a3415ebc969543aeaaf8fe816c1600b1 |
| Source note | uspto-grants-1996_12 |