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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369147Generated: October 27, 2026

Ethyl 4-phenylbenzoylformate → 5-[(1,1'-biphenyl)-4-yl]-4-hydroxy-3-phenylmethoxy-5-phenyl-2(5H)-furanone

https://huagongshe.com/reaction/369147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-phenylbenzoylformateHCID 80389—
Reactant3,4-dihydroxy-5-methyl-5-phenyl-2(5H)-furanoneHCID 54725499—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product5-[(1,1'-biphenyl)-4-yl]-4-hydroxy-3-phenylmethoxy-5-phenyl-2(5H)-furanoneHCID 5472359020%

Reaction Steps

A total of 3.4 mL (10.2 mmol) of 3.0M phenylmagnesium bromide was added to a solution of 2.4 g (10 mmol) of ethyl 4-phenylbenzoylformate in THF in an analogous manner as described for the synthesis of 3,4-dihydroxy-5-methyl-5-phenyl-2(5H)-furanone to give prior to hydrogenolysis 0.88 g (20% yield) of 5-[(1,1'-biphenyl)-4-yl]-4-hydroxy-3-phenylmethoxy-5-phenyl-2(5H)-furanone as an off white solid: mp 190-195° C. (CHCl3 /hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136832
Source datasetuspto-grants-2000_10
ORD IDord-c248f55b55b84f4aaf171965e60ca8b0
Source noteuspto-grants-2000_10