HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 13923710, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2-(2-hydroxyethyl)-N-(1,1-dimethylethyl)benzenesulfonamide | HCID 13822972 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13923710 | HCID 13923710 | — |
Reaction Steps
A suspension of 37.0 g of potassium t-butoxide in 400 ml dry tetrahydrofuran was cooled to 0° and a solution of 39.2 g of the product from Example 1 in 300 ml tetrahydrofuran was added dropwise. After the addition was complete, the reaction mixture was stirred at room temperature for 1 hour. After cooling to 0°, 9.3 ml of methyl iodide was added dropwise and the mixture stirred for 15 minutes at 0°. The solution was diluted with ether, washed with water and dried (Na2SO4). Concentration gave a viscous brown oil which was used in the following example, without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04699650 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-5710283c6a0b4df9b3b2ee241c7c6960 |
| Source note | uspto-grants-1987_10 |