HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75798Generated: October 28, 2026
Hydroxyamine hydrochloride → HCID 59034617, compound
https://huagongshe.com/reaction/75798
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3-Methyl-4-nitrobenzaldehyde | HCID 11194528 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59034617 | HCID 59034617 | — |
Reaction Steps
To a warm solution of 3-methyl-4-nitrobenzaldehyde (1.0 equiv.) in methanol was added hydroxylamine hydrochloride (2.0 equiv.) and the mixture was stirred at 65° C. for 2 hours. Methanol was evaporated and the residue was diluted with ethyl acetate. The organic layer was washed with water, brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was then recrystallized from ethyl acetate and petroleum ether 60-80, to provide the title compound as a creamish solid (81%); 1H NMR (300 MHz, CDCl3) δ: 2.62 (s, 3H), 7.54-7.56 (m, 2H), 7.89 (s, 1H), 7.98-8.01 (d, J=9.0 Hz, 1H), 8.14 (s, 1H); IR (KBr) 3375, 3207, 3087, 2994, 1607, 1585, 1506, 1384, 1319, 1161, 986, 841, 755 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835428B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-110b88133b064c6e92bebe98f59d1ccc |
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| Source note | uspto-grants-2014_09 |
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