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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475259Generated: October 31, 2026

p-(Trifluoromethoxy)benzaldehyde → 4-(trifluoromethoxy)benzaldehyde oxime

https://huagongshe.com/reaction/1475259

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(Trifluoromethoxy)benzaldehydeHCID 69573—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventMethanolHCID 887—
Product4-(trifluoromethoxy)benzaldehyde oximeHCID 958215393%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 4-(trifluoromethoxy)benzaldehyde (9.5 g, 50 mmol) and hydroxylamine hydrochloride (5.3 g, 75 mmol) in methanol (80 mL) was heated at 65° C. for 2 h. The volatiles were removed under reduced pressure and the residue was dissolved in EtOAc, and washed with H2O, brine. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The solid thus obtained was then recrystallized from EtOAc and petroleum ether to afford the title compound (9.5 g, 93%) as an off-white solid. 1H NMR (500 MHz, CDCl3) δ 8.08 (s, 1H), 7.52 (d, J=7.2 Hz, 2H), 7.15 (d, J=6.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018380B2
Source datasetuspto-grants-2015_04
ORD IDord-f6438604172d475fb5707ac7656662ab
Source noteuspto-grants-2015_04