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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422337Generated: October 30, 2026

2′-Bromo[1,1′-biphenyl]-4-carboxaldehyde → HCID 1394315, compound

https://huagongshe.com/reaction/1422337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2′-Bromo[1,1′-biphenyl]-4-carboxaldehydeHCID 1392761—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHCID 1394315HCID 1394315—

Reaction Steps

To a solution of 4-(2'-bromophenyl)benzaldehyde 1.55 g, 7.95 mmol) in ethanol (15 mL) at 0° C. was added sodium borohydride (2.22 g, 58.7 mmol) and the reation stirred for 1 hour. The reaction was quenched with saturated aq. NH4Cl and extracted into diethyl ether. The organic extracts were washed with brine, dried, (Na2SO4) and evaporated in vacuo. The residue was purified by chromatography (Silica gel, 25% EtOAc in hexanes) to afford the title compound as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080870
Source datasetuspto-grants-2000_06
ORD IDord-9015b6a7c8b84a6f920c8287ce69a7e8
Source noteuspto-grants-2000_06