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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164435Generated: October 31, 2026

3-Benzoylbenzaldehyde → HCID 13102753, compound

https://huagongshe.com/reaction/2164435

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BenzoylbenzaldehydeHCID 13020168—
ReactantHCID 178418486HCID 178418486—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13102753HCID 13102753—

Reaction Steps

Ethynylmagnesium bromide (11.2 mmol) in tetrahydrofuran (20 cm3) was added dropwise to a stirred solution of 3-benzoylbenzaldehyde (2 g, 9.5 mmol, prepared as in Example 3(b) in tetrahydrofuran (30 cm3) through which purified acetylene was being passed. After 2 hours, saturated ammonium chloride solution (200 cm3) was added, and the mixture extracted with ether (3×50 cm3). The combined extracts were washed with saturated sodium chloride, dried over anhydrous sodium sulphate, and the solvent removed in vacuo. The product was purified by thin layer chromatography on silica to give the title alcohol, yield 1.1 g (49%) nD20 1.6075.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504491
Source datasetuspto-grants-1985_03
ORD IDord-b6af8858aa2d42aeb42065e78db42027
Source noteuspto-grants-1985_03