Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 135749800 | HCID 135749800 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19735547 | HCID 19735547 | — |
Reaction Steps
After 500 mg (0.10 mmol) of Compound o obtained in Reference Example 14 was dissolved in 20 ml of tetrahydrofuran, 0.08 g (0.20 mmol) of 60% sodium hydroxide was added to the solution under ice cooling. After 30 minutes, 0.125 ml (0.20 mmol) of methyliodide was added, and the mixture was stirred for 2 hours at 50° C. The solvent was evaporated under reduced pressure, and water was added to the residue. The mixture was extracted with chloroform, and the extract was washed with a saturated aqueous sodium chloride, dried over anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure, and the residue was purified by silicagelcolumchromatography (eluent: chloroform) to afford 300 mg (yield, 58%) of Compound p as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270316 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-f8ff87a196bc4a76bf01d2a58a5da195 |
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| Source note | uspto-grants-1993_12 |
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