76129-34-5

Upstream product

• 4490-82-8 butoxyamine hydrochloride 
• 100-52-7 benzaldehyde 
• 109-65-9 1-bromo-butane 
• 622-32-2 (Z)-benzaldehyde oxime 
• 932-90-1 syn-benzaldehyde oxime 

Downstream Products

• 21855-35-6 N-(1-[2-propen-1-yl]-3-buten-1-yl)benzenamine 
• 97021-73-3 N-<1-Phenyl-pentyl-(1)>-O-butyl-hydroxylamin 
• 21855-34-5 1-Butoxyamino-1-phenyl-buten-⁽³⁾ 
• 21855-37-8 1-Butoxyamino-1-phenyl-hexen-⁽³⁾ 
• 21855-36-7 1-Butoxyamino-1-phenyl-2-ethylbuten-⁽³⁾ 
• 21855-39-0 [2-Ethyl-1-(1-ethyl-allyl)-but-3-enyl]-phenyl-amine 
• 21855-38-9 1-(Pent-2-enylamino)-1-phenylhex-3-en 

Relevant academic research and scientific papers

One-pot synthesis of oxime ethers from benzaldehyde or acetophenone, hydroxylamine salt, potassium hydroxide, and alkyl halides

Oxime ethers were synthesized in one-pot reaction from benzaldehyde or acetophenone, hydroxylamine hydrogen chloride, alkyl halides and KOH in aqueous DMSO. The reactions were completed in 15-50 min with yields in 80-96%.

THE PREPARATION OF OXIME ETHERS UNDER PHASE TRANSFER CONDITION

O-Butyloximes, O-allyloximes, O-2-chloroethyloximes, and O,O'-methylenedioximes were prepared from the corresponding oximes and halides under the phase transfer condition using sodium hydroxide and tetrabutylammonium bromide.