Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 69820608 | HCID 69820608 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18537656 | HCID 18537656 | 168.8% |
Reaction Steps
To a suspension of sodium hydride (55 wt. %, 1.26 g) in anhydrous N,N-dimethylformamide (100 ml) was added N-[5-(4-t-butoxycarbonylaminophenoxy)-2-nitrophenyl]-N-methylcarbamate (12.1 g). The mixture was stirred at ambient temperature for several minutes. To the mixture was added hexyl bromide (6.5 g) under ice cooling and the mixture was stirred at the same temperature for 30 minutes and then at room temperature for 1.0 hour. The reaction mixture was concentrated and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by chromatography on a silica gel column using toluene/diisopropyl ether=100/7 as the eluant to give the title compound (13.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432993B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-adc5012f85c64e84b4f320e6ceb51ee5 |
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| Source note | uspto-grants-2002_08 |
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