Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 54387463 | HCID 54387463 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 86738817 | HCID 86738817 | — |
Reaction Steps
A solution of 500 mg of benzyl [1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]-carbamoyl]-1-methyl-ethyl]carbamate (1.043 mol) and 150 mg of potassium t-butanolate in 20 ml of t-butanol is treated with 0.15 ml of methyl iodide and stirred at room temperature for 2.5 days. The reaction mixture is buffered with glacial acetic acid and concentrated. The residue is partitioned between methylene chloride and 10 percent aqueous sodium bicarbonate solution. After drying the organic phase overnight and concentrating, the residue is chromatographed on a pressure column containing 10 g of silica gel (particle size 0.04-0.06 mm) under 0.2-0.4 atmospheres of nitrogen with methylene chloride/ethyl acetate (20:1) as the elution agent. There is obtained benzyl [1-[[2-(o-fluorobenzoyl)-4-nitrophenyl]-methylcarbamoyl]-1-methyl-ethyl]carbamate of melting point 168°-169° (ether/n-hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377522 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-5bd29afbb2c34d7bbdecb7cc5192ee0c |
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| Source note | uspto-grants-1983_03 |
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