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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369145Generated: October 27, 2026

Chloroform → 5-[(1,1'-biphenyl)-4-yl]-4-hydroxy-3-phenylmethoxy-5-(2-methylpropyl)-2(5H)-furanone

https://huagongshe.com/reaction/369145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantEthyl 4-phenylbenzoylformateHCID 80389—
Reactant3,4-dihydroxy-5-methyl-5-phenyl-2(5H)-furanoneHCID 54725499—
ReactantHCID 178418816HCID 178418816—
SolventTetrahydrofuranHCID 8028—
Product5-[(1,1'-biphenyl)-4-yl]-4-hydroxy-3-phenylmethoxy-5-(2-methylpropyl)-2(5H)-furanoneHCID 547235958%

Reaction Steps

A total of 5.2 mL (10.4 mmol) of 2.0M isobutylmagnesium 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 0.35 g (8% yield) of 5-[(1,1'-biphenyl)-4-yl]-4-hydroxy-3-phenylmethoxy-5-(2-methylpropyl)-2(5H)-furanone as an off white solid after crystallization from CHCl3 and hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136832
Source datasetuspto-grants-2000_10
ORD IDord-e09b2aeb9db64685868dd803566f4889
Source noteuspto-grants-2000_10