HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → N-allyl-N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide | HCID 20152991 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-allyl-N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide | HCID 14097714 | — |
Reaction Steps
To N-(2-trifluoromethylphenyl)-2-pyridinesulfonamide 1-oxide (compound 129, Table A) (1.0 g, 3.0 mmol) in 10 ml of DMF is added NaH (0.30 g, 6.2 mmol) under N2, and the mixture is stirred at RT for 30 minutes. Allyl bromide (0.82 g, 0.59 ml, 6.8 mmol) is added dropwise, and the mixture is stirred at RT for 48 hours. It is then worked up and purified to give the title compound (compound 37, Table A). (DMF is dimethylformamide; RT is room temperature.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04722749 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-032d77276ec347c0b8611cfd56e26b51 |
| Source note | uspto-grants-1988_02 |