HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572677Generated: October 25, 2026
Hydroxyamine hydrochloride → 6-Bromo-2-methylpyrimidine-4-carbaldehyde oxime
https://huagongshe.com/reaction/572677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Diacetate | HCID 23662384 | — |
| Reactant | 6-Bromo-2-methylpyrimidine-4-carbaldehyde | HCID 86675929 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Bromo-2-methylpyrimidine-4-carbaldehyde oxime | HCID 136413233 | 33.8% |
Reaction Steps
To a stirred solution of 6-bromo-2-methylpyrimidine-4-carbaldehyde (11 g, 54.7 mmol, Preparation #17 step 1) and NH2OH.HCl (7.61 g, 109 mmol, Sisco Research Labs) in ethanol (75 mL) and water (25 mL) was added sodium acetate acetate (13.47 g, 164 mmol). The reaction mixture was heated to reflux at about 90° C. for about 1 h. The mixture was cooled to RT and diluted with water (200 mL). The separated product (solid) was collected by filtration, washed with water and dried under vacuum to afford 6-bromo-2-methylpyrimidine-4-carbaldehyde oxime 4.0 g (33.8%), 1H NMR (400 MHz, DMSO) δ: 12.43 (s, 1H), 8.01 (s, 1H), 7.78 (s, 1H), 2.61 (s, 3H), MS m/z: 216 (negative mode).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029409B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-9eb1ee3269684dae9f81e4efe5659cd3 |
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| Source note | uspto-grants-2015_05 |
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