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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573783Generated: October 26, 2026

2-Iodoxybenzoic acid → 3-Isobutyryl-1,8-dioxaspiro[4.5]dec-3-en-2-one

https://huagongshe.com/reaction/573783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodoxybenzoic acidHCID 108794—
Reactant4-Methoxypyridine N-oxide hydrateHCID 16212293—
Reactant3-Isobutyryl-1,8-dioxaspiro[4.5]decan-2-oneHCID 66761804—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
Product3-Isobutyryl-1,8-dioxaspiro[4.5]dec-3-en-2-oneHCID 66762855—

Reaction Steps

2.16 g 4-Methoxypyridine-1-oxide hydrate and 5.57 g 2-iodoxybenzoic acid (45 wt-%) are suspended in 20 ml dimethylsulfoxide and stirred for 20 minutes until all material has dissolved. Then 3.0 g 3-isobutyryl-1,8-dioxaspiro[4.5]decan-2-one are added and the mixture is stirred for 24 hours. The mixture is diluted with saturated solution of sodium bicarbonate in water and the formed precipitate is filtered off. The mother liquor is extracted for three times with ethylacetate. The combined organic phases are dried with sodium sulphate and the solvents are evaporated in vacuo. The residue is chromatographed on silica gel (petrole ether/ethylacetate 100:0 to 40:60).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029544B2
Source datasetuspto-grants-2015_05
ORD IDord-6d51a94190364c88ba34cb9122f8c9ae
Source noteuspto-grants-2015_05