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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268705Generated: October 30, 2026

Benzaldehyde → HCID 21075637, compound

https://huagongshe.com/reaction/1268705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 136148285HCID 136148285—
SolventAcetic AcidHCID 176—
ProductHCID 21075637HCID 2107563724.1%

Reaction Steps

A mixture of (Z)-1(4-fluorophenyl)-2-(hydroxyimino)-2-(2-(methylthio)pyrimidin-4-yl)ethanone (0.5 g), ammonium acetate (2.7 g) and benzaldehyde (0.2 g) in acetic acid (11 mL) are heated under reflux for 4 h, cooled to room temperature and the majority of the solvent evaporated. The residue is partitioned between ice-cold saturated aqueous sodium hydrogen carbonate and ethyl acetate. The layers are separated and the aqueous phase is extracted with ethyl acetate. The combined organic phases are dried over sodium sulfate, filtered and the solvent evaporated. The residue is dissolved in methanol (8 mL). This solution is treated with a solution of titanium (III) choride in hydrochloric acid (0.44 mL, 15 wt %, 20–30% hydrochloric acid), followed by stirring at room temperature for 3 h and solvent evaporation. The residue is partitioned between ice-cold saturated aqueous sodium hydrogen carbonate and ethyl acetate, then the layers are separated and the aqueous phase is extracted with ethyl acetate. The combined organic phases are dried over sodium sulfate, filtered, the solvent evaporated and the residue purified by chromatography to give the title compound, 75 (0.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199126B2
Source datasetuspto-grants-2007_04
ORD IDord-412778388d2f4107abd44cba639dc546
Source noteuspto-grants-2007_04