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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786783Generated: October 29, 2026

4-Fluorobenzaldehyde → 4-Fluoro-benzaldehyde O-methyl-oxime

https://huagongshe.com/reaction/1786783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium AcetateHCID 517045—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4-Fluoro-benzaldehyde O-methyl-oximeHCID 53963238100.2%

Reaction Conditions

Temperature22 °C

Reaction Steps

A solution of methoxylamine hydrochloride (13.4 g, 0.16 mol) in a mixture of water (150 ml) and tetrahydrofuran (50 ml) was treated with sodium acetate (11.2 g, 0.136 mol) followed by 4-fluorobenzaldehyde (11.57 g, 93.2 mmol) and the resulting mixture was stirred at 22° C. for 4 hours. The reaction mixture was then diluted with ether, washed with brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure gave 14.3 g of the crude title material as a clear oil which was used as such for the next step. Distillation of an aliquot in vacuo gave a clear oil; bp 45-50° C./0.5 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507838B2
Source datasetuspto-grants-2009_03
ORD IDord-1d82c1f3015a448a8509276700ce7f95
Source noteuspto-grants-2009_03