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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant3-Bromo-2-(tert-butylthio)benzaldehydeHCID 86662397—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product1-[3-bromo-2-(tert-butylsulfanyl)phenyl]-N-hydroxymethanimineHCID 86662398—

Reaction Conditions

Temperature67.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-1c5ca2ddc72f4b629ae272aa4eecacfc
Source noteuspto-grants-2013_02