HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374956Generated: October 25, 2026
Sodium Hydroxide → 2-Methoxy-5-(1-methyl-cyclopropyl)-benzene-1,3-diamine
https://huagongshe.com/reaction/1374956
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 2-Methoxy-5-(1-methyl-cyclopropyl)-1,3-dinitro-benzene | HCID 17973071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Methoxy-5-(1-methyl-cyclopropyl)-benzene-1,3-diamine | HCID 17973087 | 52% |
Reaction Steps
Tin(II)chloride dihydrate (11.9 g, 52.6 mmol) was added to a solution of 2-methoxy-5-(1-methyl-cyclopropyl)-1,3-dinitro-benzene (2.21 g, 8.76 mmol) in ethyl acetate (30 mL). The mixture was heated to reflux for 0.25 h upon which the solution became red in color. The solution was cooled to rt and poured onto aqueous 2.0 M NaOH. The aqueous phase was extracted with ethyl acetate and the combined organic layers were washed with saturated NaHCO3. The organic layers were dried over sodium sulfate, eluted through a plug of silica gel (1% ammonium hydroxide in methylene chloride), and the filtrate was concentrated. The residue was redissolved in Et2O and extracted (3×) with 1.0 M HCl. The pH of the combined aqueous layers was adjusted to pH=12 with 2.0M NaOH and extracted with methylene chloride. The combined organic layers were dried over sodium sulfate, filtered and concentrated to provide 2-methoxy-5-(1-methyl-cyclopropyl)-benzene-1,3-diamine (860 mg, 52%) as a red oil. ESI MS (m/z 193, M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166628B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-7ba2e898abb84726a52d0f28cc1a354f |
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| Source note | uspto-grants-2007_01 |
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