Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216184Generated: November 1, 2026

Pyridine → 4-Bromo-5-nitro-thiophene-2-carbaldehyde oxime

https://huagongshe.com/reaction/2216184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant4-Bromo-5-nitrothiophene-2-carbaldehydeHCID 21886281—
SolventEthanolHCID 702—
Product4-Bromo-5-nitro-thiophene-2-carbaldehyde oximeHCID 7385215288%

Reaction Steps

Hydroxylamine hydrochloride (85 g, 1.2 mol) was added to a solution of 4-bromo-5-nitro-thiophene-2-carbaldehyde (234 mg, 0.529 mmol, Example 286: step a) in EtOH (7.5 mL, 200 proof—anhydrous):pyridine (100 mL, anhydrous) at rt over 5 min. The reaction mixture was heated to reflux overnight, then cooled to rt. The solvents were removed in vacuo resulting in a solid residue that was washed with water and filtered. The solid was dried overnight under high vacuum to afford the title compound as a yellow solid (225 g, 88%). The solid was used for the next step without further characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109354B2
Source datasetuspto-grants-2006_09
ORD IDord-593ab75ba96d4ed096ac1ee64977a991
Source noteuspto-grants-2006_09