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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369138Generated: October 28, 2026

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

https://huagongshe.com/reaction/369138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-phenylbenzoylformateHCID 80389—
Reactant3,4-dihydroxy-5-methyl-5-phenyl-2(5H)-furanoneHCID 54725499—
ReactantHCID 178418373HCID 178418373—
SolventTetrahydrofuranHCID 8028—
Product5-[(1,1'-biphenyl)-4-yl]-3-phenylmethoxy-4-hydroxy-5-methyl-2(5H)-furanoneHCID 5471875530%

Reaction Steps

A total of 3.4 mL (10.2 mmol) of 3.0M methylmagnesium iodide in THF was added to a THF solution of 2.4 g (10 mmol) of ethyl 4-phenylbenzoylformate 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, 1.1 g (30% yield) of 5-[(1,1'-biphenyl)-4-yl]-3-phenylmethoxy-4-hydroxy-5-methyl-2(5H)-furanone as a white granular solid: m.p. 182-183° C. (benzene/hexanes) 1H NMR (CDCl3) δ 7.56-7.26 (m, 14H), 5.10 (ab quartet, 2H, J=11.4 Hz), 1.79 (s, 3H). 13C NMR (CDCl3) δ 168.5, 163.8, 141.5, 140.3, 137.0, 136.3, 129.0, 128.8, 128.8, 128.8, 127.6, 127.2, 127.1, 125.6, 119.0, 81.1, 73.5, 24.3. Anal Calcd for C24H20O4 : C, 77.40; H, 5.41. Found: C, 77.99; H, 5.61.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136832
Source datasetuspto-grants-2000_10
ORD IDord-3d210714a17d42dc937fc632dfedec31
Source noteuspto-grants-2000_10