HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339472Generated: October 26, 2026
Stannous Chloride → 5-Bromo-2-cyclopropylaniline
https://huagongshe.com/reaction/339472
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 4-Bromo-1-cyclopropyl-2-nitrobenzene | HCID 671343 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-2-cyclopropylaniline | HCID 4712248 | — |
Reaction Steps
Tin (II) chloride (16.0 g, 0.10 mol) is added in one portion to a solution of crude 5-bromo-2-cyclopropylnitrobenzene (8.68 g) in ethanol (190 ml) and water (1.9 ml). The reaction mixture is stirred at room temperature overnight, followed by addition of further tin (II) chloride (28 g, 0.175 mol) and additional stirring overnight. After concentration in vacuo ice is added, and the solution is basified with 2M aqueous sodium hydroxide. After extraction with ethyl acetate (×2) the organic phase is washed again with 2M aqueous sodium hydroxide, then also distilled water and brine. After drying over magnesium sulfate the solution is concentrated in vcauo to give a brown oil which is purified by flash column chromatography on silica gel (9:1 isohexane/ethyl acetate eluant) to afford 5-bromo-2-cyclopropylaniline as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895474B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-f0c62ef52de1426aabf80164a404c482 |
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| Source note | uspto-grants-2014_11 |
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