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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111755Generated: October 26, 2026

Sodium Hydroxide → 3-Bromo-thiophene-2-carbaldehyde oxime

https://huagongshe.com/reaction/2111755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant3-Bromothiophene-2-carboxaldehydeHCID 2797079—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-Bromo-thiophene-2-carbaldehyde oximeHCID 73016922.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Bromothiophene-2-carbaldehyde (28.7 g, 0.15 mol) in ethanol (50 mL) was added in one portion to a solution of hydroxylamine hydrochloride (13.8 g, 0.2 mol), sodium hydroxide (8 g, 0.2 mol) in water (30 mL) and ethanol (100 mL). The mixture was stirred at 0° C. for 2 hours and was kept at 0° C. overnight when a precipitate formed. The mixture was diluted with cold water (600 ml) and the solid was collected by filtration yielding 20.5 g, (67%). The aqueous solution was further extracted with ethyl acetate. The organic solution was washed with brine, dried with magnesium sulfate, filtered and evaporated yielding 6.9 g of additional product as a light yellow solid. The total yield was 27.4 g (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521445B2
Source datasetuspto-grants-2009_04
ORD IDord-6c5fdba8bbf343b288c5e9dac1bb4cde
Source noteuspto-grants-2009_04