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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417745Generated: November 2, 2026

Tetrahydrofuran → Benzaldehyde, 4-amino-, oxime

https://huagongshe.com/reaction/1417745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactantp-NitrobenzaldoximeHCID 96339—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
ProductBenzaldehyde, 4-amino-, oximeHCID 102410—

Reaction Steps

8.3 g of 4-nitrobenzaldoxime together with 100 ml of tetrahydrofuran are initially introduced into a stirred autoclave. 50 mg of FeCl2.4 H2O and 0.2 g of the catalyst from Example A1 are added to the solution. Hydrogenation is carried out at 120° C. and a hydrogen pressure of 20×105 pascals. When hydrogenation is complete, the mixture is cooled to room temperature, the reactor is rendered inert with nitrogen and the catalyst is filtered off. The solvent is distilled off to give, after chromatographic purification, 3.5 g (51% of theory) of 4-aminobenzaldoxime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877340
Source datasetuspto-grants-1999_03
ORD IDord-9eb092de73ae4d899d1819ce918f89d7
Source noteuspto-grants-1999_03