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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333198Generated: October 31, 2026

1,3-Dibenzoylbenzene → HCID 85856804, compound

https://huagongshe.com/reaction/333198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibenzoylbenzeneHCID 77388—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHCID 85856804HCID 8585680430%

Reaction Conditions

Temperature0 °C

Reaction Steps

1,3 dibenzoylbenzene 2 (2.00 g, 6.98 mmol) was dissolved in anhydrous ethanol (20 mL) under an inert atmosphere of nitrogen gas. The reaction mixture was cooled to 0° C. followed by the addition of sodium borohydride (0.090 g, 2.094 mmol). The reaction mixture was stirred for 4 h and quenched the addition of a small amount of water. The reaction mixture was concentrated under reduced pressure and the products were extracted from water with ethyl acetate (2×50 mL). The combined organic phases were washed with brine, dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. Purification using flash chromatography (silica gel, hexanes:ethyl acetate, gradient 93:7 to 30:70) afforded 3-benzoyl benzhydrol 5 (0.601 g, 2.084 mmol) in a 30% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877967B2
Source datasetuspto-grants-2014_11
ORD IDord-61a944f91f9940deb26073d7f1eed2ec
Source noteuspto-grants-2014_11