Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18703994 | HCID 18703994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18703989 | HCID 18703989 | 96% |
Reaction Steps
A solution of 0.5 g (1.6 mmol) of methyl 5-methanesulfonylamino-7,7-dimethyl-5,6,7,8-tetrahydro-1-naphthalenecarboxylate in 5 ml of DMF was added dropwise to a suspension of 0.05 g (1.8 mmol) of 80 percent sodium hydride in 4 ml of DMF. After stirring at room temperature for 1 hr., 0.23 g (1.6 mmol) of iodomethane was added and the mixture was stirred at room temperature for 4 h. The reaction mixture was completely concentrated in vacuo and the residue was then taken up in EA and water and the organic phase was washed with dilute hydrochloric acid and sodium bicarbonate solution. After drying over magnesium sulfate and concentrating in vacuo; 0.5 g of methyl 5-(methanesulfonyl-methyl-amino)-7,7-dimethyl-5,6,7,8-tetrahydronaphthalene-1-carboxylate was obtained; m.p. 98-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06087399 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-f1f151a54dcd48dfb0458c76c0770eaf |
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| Source note | uspto-grants-2000_07 |
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