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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385029Generated: November 1, 2026

2-Iodonaphthalene → HCID 54723593, compound

https://huagongshe.com/reaction/1385029

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodonaphthaleneHCID 136412—
ReactantHCID 54703388HCID 54703388—
ReactantHCID 54723600HCID 54723600—
ProductHCID 54723593HCID 5472359378.2%

Reaction Steps

5-(3-Butynyl)-3,4-dihydroxy-2(5H)-furanone (0.1 7 g, 1.0 mmol) and 3 00 μL (2.0 mmol) of 2-iodonaphthalene were coupled in an analogous fashion as described for the synthesis of 3,4-dihydroxy-5-[(4-phenyl)-3-butynyl]-2(5H)-furanone. The residue was purified over silica gel using CHCl3/MeOH/AcOH (96/3/1) as eluant and dried at 0.05 mm Hg at 58° C. for 2 h to provide 230 mg (75%) of 3,4-dihydroxy-5-[4-(2-naphthyl)-3-butynyl]-2(5H)-furanone as a yellow wax: 1H NMR (acetone-d6) δ 8.4-8.3 (m, 1H), 7.96-7.88 (m, 2H), 7.70-7.43 (m, 4H), 4.98 (dd, J=3.4, 8.3 Hz, 1H), 2.82-2.75 (m, 2H), 2.48-2.29 (m, 1H), 2.00-1.85 (m, 1H); Anal Calcd for C18H14O4+0.5 H2O: C, 71.27; H, 4.98. Found: C, 71.33; H, 4.87.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262073B1
Source datasetuspto-grants-2001_07
ORD IDord-ae6615f5304247ba89dc5e0247fb7133
Source noteuspto-grants-2001_07