HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-(Trifluoromethyl)benzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Trifluoromethylbenzenesulphonyl chloride | HCID 136616 | — |
| Reactant | 2-Chloro-6-methylbenzene-1-sulfonyl chloride | HCID 15725370 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2733250 | — |
Reaction Steps
2-Chloro-6-methylbenzenesulfonyl chloride (8, 7.82 g, 34.8 mmol) was added to a solution of 7 (8.83 g, 31.6 mmol) in pyridine (7.67 ml, 95.0 mmol) and the reaction mixture was stirred at room temperature overnight. CH2Cl2 and H2O were added to the reaction mixture and the organic phase was separated, washed with water and sat. NaCl solution, dried over Na2SO4 and concentrated to obtain the product 9, which was employed directly as such in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318769B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-95cbadb8c3bb41a2be08fd8d9b9cf1ad |
| Source note | uspto-grants-2012_11 |