HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875226Generated: November 5, 2026
Hydroxyamine hydrochloride → HCID 86650757, compound
https://huagongshe.com/reaction/875226
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 66887902 | HCID 66887902 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86650757 | HCID 86650757 | — |
Reaction Steps
A solution of (1-methyl-1H-imidazol-5-yl)(3-thienyl)methanone (11.6 g, 60.0 mmol) and hydroxylamine hydrochloride (14.6 g, 210 mmol) in pyridine (60 mL) was stirred 9 h at 60° C. then left to stand for 72 h at room temperature. After removal of the solvent in vacuo, addition of water (200 mL), pH adjustment to approx 7 with aq. NaOH (1 M) induced precipitation of a solid. Filtration, sequential washings of the precipitate with water and heptane, and drying of the solid afforded a first crop of N-hydroxy-1-(1-methyl-1H-imidazol-5-yl)-1-(3-thienyl)methanimine. The combined aqueous phases were extracted with dichloromethane, the combined organic layers were dried over MgSO4 and concentrated in vacuo. The residue was purified recrystallized from heptane to afford a second crop of N-hydroxy-1-(1-methyl-1H-imidazol-5-yl)-1-(3-thienyl)methanimine. The crops were combined and recrystallized from diisopropylether to afford final N-hydroxy-1-(1-methyl-1H-imidazol-5-yl)-1-(3-thienyl)methanimine [9.95 g, yield 76%; HPLC/MS m/z=208 (M+H); log P(HCOOH)=0.21].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08981111B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-9ef21242bbb64ecb829747c13f46474c |
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| Source note | uspto-grants-2015_03 |
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