HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259907Generated: October 31, 2026
Sodium hydride → 5-fluoro-N-(4-methoxybutyl)-2-nitroaniline
https://huagongshe.com/reaction/1259907
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Fluoro-2-nitroaniline | HCID 75399 | — |
| Reactant | 4-Methoxybutyl methanesulfonate | HCID 11687006 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 5-fluoro-N-(4-methoxybutyl)-2-nitroaniline | HCID 58355755 | 31.8% |
Reaction Steps
5-Fluoro-2-nitroaniline (1.0 g) was dissolved in THF (20 ml), sodium hydride (60% in oil, 384 mg) was added, and the mixture was stirred at room temperature for 30 min. 4-Methoxybutyl methanesulfonate (1.28 g) was added, and the mixture was heated under reflux with stirring for 15 hr. The reaction mixture was cooled to room temperature and saturated brine was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (30:70) was concentrated under reduced pressure to give the object product (494 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466282B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-ce56c47c066542ae9e8a4b2b4621dcc9 |
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| Source note | uspto-grants-2013_06 |
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