HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189053Generated: November 1, 2026
Hydroxyamine hydrochloride → HCID 75182053, compound
https://huagongshe.com/reaction/1189053
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3-[(6-Methylpyridin-2-yl)ethynyl]cyclohex-2-en-1-one | HCID 68936731 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 75182053 | HCID 75182053 | 42.4% |
Reaction Steps
A solution of 3-(6-methyl-pyridin-2-ylethynyl)-cyclohex-2-enone (422 mg, 2 mmol) and hydroxylamine hydrochloride (278 mg, 4 mmol) in pyridine (20 ml) is stirred for 17 h at RT. After that time the solvent is evaporated in vacuo. The residue is dissolved in ethyl acetate (300 ml) and washed with sat NaHCO3 (1×50 ml). The water phase is extracted with ethyl acetate (1×50 ml). The combined organic phases are dried over Na2SO4, filtered and concentrated in vacuo. The residue (0.45 g) is purified on column chromatography (Silica gel, eluent hexane/ethyl acetate 2:1 v/v) and the fractions containing the desired compound are collected and concentrated in vacuo to yield 0.192 g (yield=42%) of the title compound as light yellow crystals, m.p. 166-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674110B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-1e74ce7b79e341b896c5db298ac0559d |
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| Source note | uspto-grants-2014_03 |
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