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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005707Generated: October 31, 2026

Benzaldehyde → HCID 22674379, compound

https://huagongshe.com/reaction/1005707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium hydrideHCID 24758—
Reactant1,1-Dimethyl-1H-imidazol-1-ium iodideHCID 13685884—
Reactant4-Chloro-2-(trifluoromethyl)thieno(3,2-d)pyrimidineHCID 22674373—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22674379HCID 2267437972.1%

Reaction Steps

A suspension of 4-chloro-2-trifluoromethylthieno[3,2-d]pyrimidine (0.3 g, 1.26 mmol), benzaldehyde (0.28 g, 2.64 mmol) and N,N-dimethylimidazolium iodide (0.2 g, 0.89 mmol) in THF (8 mL) was treated with NaH (60% dispersion in oil, 0.112 g, 2.8 mmol), refluxed for 15 min, cooled to room temperature, treated with water (4 mL) and the organic phase separated. The aqueous phase was extracted with CH2Cl2 (2×20 mL), the combined organic phase washed with brine (10 mL), dried (MgSO4), concentrated in vacuo and the resulting brown oil purified by chromatography [SiO2; heptane-EtOAc (3:1)] then recrystallised from heptane to give the title compound (280 mg, 43%) as yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787541B1
Source datasetuspto-grants-2004_09
ORD IDord-2c70b2d3400a463ebfde38c88cd8187e
Source noteuspto-grants-2004_09