HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 19107600, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 19107610 | HCID 19107610 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19107600 | HCID 19107600 | — |
Reaction Steps
Sodium hydride (60% dispersion in oil: 190 mg, 4.7 mmol) was added to a stirred solution of N-1,2-diphenylethyl 4-bromomethylbenzenesulphonamide (2.00 g, 4.7 mmol) in dry THF (50 ml) at 0° C. under argon. Methyl iodide (0.6 ml, 9.3 mmol) was added immediately to the reaction mixture. The mixture was stirred for 48 h at ambient temperature. Saturated aqueous ammonium chloride (50 mi) was added and the mixture extracted with ethyl acetate (2×80 ml). The combined organics were washed with brine (50 ml), dried over anhydrous sodium sulphate, filtered and concentrated to give N-methyl-N-1,2-diphenylethyl 4-bromomethylbenzenesulphonamide as an orange oil which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05276153 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-b865332524244c0d8c65ab7dfeab9e5d |
| Source note | uspto-grants-1994_01 |