HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697442Generated: October 31, 2026
Hydrazine hydrate (1:1) → o-(4-Chlorophenyl)hydroxylamine
https://huagongshe.com/reaction/1697442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-(4-Chlorophenoxy)isoindoline-1,3-dione | HCID 15370735 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | o-(4-Chlorophenyl)hydroxylamine | HCID 12571735 | — |
Reaction Steps
Hydrazine hydrate (0.56 mL, 12 mmol) was added to a solution of Example 3A (820 mg, 3.0 mmol) in chloroform (37 mL) and methanol (4 mL). The suspension was stirred at room temperature for 22 hours. Silica gel (10 g) was added, and the mixture was concentrated to dryness. The residue was applied to the top of a flash chromatography column and eluted with hexanes-ethyl acetate (80:20) to provide the title compound as the free amine. The residue was dissolved in ethanol (5 mL) and treated with HCl/dioxane (4M, 1 mL). The solution was heated at reflux and diluted with gradual addition of ethyl acetate (50 mL). The mixture was cooled to room temperature and filtered to provide the title compound as a hydrochloride salt. 1H NMR (300 MHz, CD3OD) δ 7.15-7.22 (m, 2 H), 7.42-7.49 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163915B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-d5b0d20dac0849c6ae4cb41d7105fad4 |
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| Source note | uspto-grants-2012_04 |
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