HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77567Generated: October 26, 2026
Pyridine → 1-(3-Bromophenyl)-2-(diallylamino)ethanone oxime
https://huagongshe.com/reaction/77567
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 1-(3-Bromophenyl)-2-(diallylamino)ethanone | HCID 86762750 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-Bromophenyl)-2-(diallylamino)ethanone oxime | HCID 86762751 | 119.3% |
Reaction Steps
A solution of 1-(3-bromophenyl)-2-(diallylamino)ethanone (60 g, 204.7 mmol) in ethanol (720 mL) and pyridine (24.8 mL, 307 mmol) is stirred 15 minutes at 22° C. Hydroxylamine hydrochloride (17 g, 246 mmol) is added in portions to the solution over 1 hour. The reaction is warmed to 50° C. for 2 hours and then heated to 70° C. for 16 hours. The solvent is evaporated and the residue partitioned in water (300 mL) and methyl tert-butyl ether (300 mL). The organic layer is separated and washed with water (100 mL, 2×) and brine (100 mL). The organic layer is dried over sodium sulfate, filtered, and evaporated to dryness to give the title compound (75.5 g, 79%). ES/MS (m/e): 309 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841293B1 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8b2cbcd8c51c43beafa06095d62131da |
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| Source note | uspto-grants-2014_09 |
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