HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → N-(tert-butyl)-2-iodo-6-methoxybenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | N-(tert-butyl)-2-methoxybenzenesulfonamide | HCID 23448664 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(tert-butyl)-2-iodo-6-methoxybenzenesulfonamide | HCID 23151662 | — |
Reaction Conditions
| Temperature | -30 °C |
|---|
Reaction Steps
A solution of 30.00 g (123.29 mmol) of N-(tert-butyl)-2-methoxybenzenesulfonamide in 400 ml of tetrahydrofuran is cooled to −70° C. and slowly admixed with a solution of 110.96 ml (277.41 mmol) of a 2.5 molar n-butyllithium solution in THF. The solution is subsequently warmed briefly to −30° C. and then cooled again to −60° C. At this temperature a solution of 31.29 g (123.29 mmol) of iodine in 200 ml of tetrahydrofuran is added dropwise. Subsequently the reaction solution is stirred at room temperature overnight. Following extraction with water, the organic phase is dried over sodium sulfate and evaporated to dryness. This gives 42.40 g (93% of theory) of N-(tert-butyl)-2-iodo-6-methoxybenzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855166B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-3f93c616012f444e9f01790214c63b9c |
| Source note | uspto-grants-2010_12 |