Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Bromide | HCID 6323 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 3856345 | HCID 3856345 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22164290 | HCID 22164290 | 87% |
Reaction Steps
27.5 g (0.1 mole) of N-(α,α-dimethylbenzyl)benzenesulfonamide was added to 5.8 g (0.12 mole) of 50% sodium hydride in 200 ml of dry N,N-dimethyl formamide. The mixture was stirred at room temperature for 30 minutes to react them. To the resulting sodium salt of N-(α,α-dimethylbenzyl)benzenesulfonamide was added 16.1 g (0.17 mole) of methyl bromide. The mixture was heated to 60° C. and stirred for 1 hours. The N,N-dimethyl formamide was distilled off under reduced pressure, and cold water was added. The resulting white solid was recrystallized from methanol to afford N-methyl-N-(α,α-dimethylbenzyl)benzenesulfonamide in a yield of 87%. This compound is designated as compound No. 64 in Table 2 below, and its melting point and elemental analysis values are shown in Table 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04233061 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-d45e57a236d24a299c67f91a1a3bb514 |
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| Source note | uspto-grants-1980_11 |
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