HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389437Generated: October 25, 2026
Hydroxyamine hydrochloride → 1-[3-bromo-2-(tert-butylsulfanyl)phenyl]-N-hydroxymethanimine
https://huagongshe.com/reaction/389437
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3-Bromo-2-(tert-butylthio)benzaldehyde | HCID 86662397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-[3-bromo-2-(tert-butylsulfanyl)phenyl]-N-hydroxymethanimine | HCID 86662398 | — |
Reaction Steps
A mixture of 3-bromo-2-tert-butylsulfanyl-benzaldehyde (6.7 g, 25 mmol) and hydroxylamine hydrochloride (7.9 g, 116 mmol) in 2-propanol (200 mL) and water (40 mL) was heated to 65-70° C. overnight. 2-Propanol was evaporated and water (150 mL) was added to the residue followed by saturated aqueous sodium bicarbonate to bring the pH to ˜8.5. The mixture was extracted with DCM (3×80 mL). The combined organic fractions were dried over sodium sulfate, filtered, and concentrated to afford the title compound, which was used immediately without further purification. 1H NMR (300 MHz, CD3OD): δ 1.28 (s, 9H), 7.25-7.35 (t, J=7.8 Hz, 1H), 7.79 (d, J=6.6 Hz, 1H), 7.89 (d, J=6.3 Hz, 1H), 8.83 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378104B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-1c5ca2ddc72f4b629ae272aa4eecacfc |
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| Source note | uspto-grants-2013_02 |
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