Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67953980 | HCID 67953980 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67954048 | HCID 67954048 | — |
Reaction Steps
8-benzyloxy-1-methyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione (33.4 g, 113 mmol), tetrabutyl ammonium bromide (7.28 g, 22.6 mmol) and an aqueous solution of 25% sodium hydroxide (20.8 g, 130 mmol) were added to the mixture of toluene (167 mL) and water (150 mL). Ethyl iodide (10.4 mL, 130 mmol) was added thereto, and the reaction was performed at 80° C. for 4 hours. The reaction solution was cooled, and ethyl acetate (334 mL) extraction was performed. The resulting organic layer was washed with water, and the solvent was distilled off under reduced pressure. Ethyl acetate (70 mL) was added to the resulting residue, and the mixture was heated and dissolved. Thereafter, hexane (35 mL) was added thereto, and heating was performed again. The mixture was stirred at 40-50° C. for 30 minutes, and stirred under ice cooling for 1 hour to collect precipitated crystals by filtration. The resulting crystals were washed with ethyl acetate-hexane (1:1; 50 mL), and dried at 60° C., thereby obtaining 39.6 g of a light-yellow, powdery target compound (containing ammonium salt).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940889B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-b54b5fded83c4c9abb9e98986cc18a65 |
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| Source note | uspto-grants-2015_01 |
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