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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369154Generated: October 28, 2026

4-hydroxy-5-(4-isobutylphenyl)-5-phenyl-3-phenylmethoxy-2(5H)-furanone → 3,4-dihydroxy-5-(4-isobutylphenyl)-5-phenyl-2(5H)-furanone

https://huagongshe.com/reaction/369154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-hydroxy-5-(4-isobutylphenyl)-5-phenyl-3-phenylmethoxy-2(5H)-furanoneHCID 54723592—
Reactant3,4-dihydroxy-5-methyl-5-phenyl-2(5H)-furanoneHCID 54725499—
Product3,4-dihydroxy-5-(4-isobutylphenyl)-5-phenyl-2(5H)-furanoneHCID 5472549751.4%

Reaction Steps

Hydrogenolysis of 500 mg (1.2 mmol) of 4-hydroxy-5-(4-isobutylphenyl)-5-phenyl-3-phenylmethoxy-2(5H)-furanone was performed in a similar manner as described in the preparation of 3,4-dihydroxy-5-methyl-5-phenyl-2(5H)-furanone to provide 200 mg (51% yield) of 3,4-dihydroxy-5-(4-isobutylphenyl)-5-phenyl-2(5H)-furanone as a white powder: mp 138-139° C. (CHCl3 /hexanes). 1H NMR (acetone-d6) δ 7.40-7.15 (m, 9H), 2.49 (d, J=7.1 Hz, 2H), 1.94-1.74 (m, 1H), 0.89 (d, J=6.5 Hz, 6H). Anal Calcd for C20H20O4 : C, 74.1; H, 6.2. Found: C, 73.7; H, 6.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136832
Source datasetuspto-grants-2000_10
ORD IDord-60a2e17287284c32959b54cb755835b9
Source noteuspto-grants-2000_10