HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258452Generated: November 2, 2026
Sodium hydride → N-[2-(Benzyloxy)-4-bromo-6-nitrophenyl]-N-(2-methoxyethyl)acetamide
https://huagongshe.com/reaction/1258452
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | N-(2-(benzyloxy)-4-bromo-6-nitrophenyl)acetamide | HCID 67220372 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[2-(Benzyloxy)-4-bromo-6-nitrophenyl]-N-(2-methoxyethyl)acetamide | HCID 67220533 | 77.1% |
Reaction Steps
To a suspension of sodium hydride (60% dispersion in mineral oil, 1.78 g, 44.5 mmol) in N,N-dimethylformamide (100 mL) was added dropwise a solution of N-[2-(benzyloxy)-4-bromo-6-nitrophenyl]acetamide (13.5 g, 37.1 mmol, Step 1) in N,N-dimethylformamide at 0° C. over 10 minutes. After stirring at 0° C. for 20 minutes, 1-bromo-2-methoxyethane (7.21 g, 51.9 mmol) was added, and the mixture was stirred at 50° C. for 2 hours. After cooling to room temperature, the mixture was poured onto water, and the aqueous layer was extracted with ethyl acetate/toluene (3:1). The combined organic layer was dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (3:1) to afford the title compound as a gray solid (12.1 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466166B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-2ffddae088974f23986f8611e078d108 |
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| Source note | uspto-grants-2013_06 |
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