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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974724Generated: October 29, 2026

Glyoxylic Acid → HCID 22628567, compound

https://huagongshe.com/reaction/974724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlyoxylic AcidHCID 760—
ReactantWaterHCID 962—
Reactant2,4-Di-tert-butylphenolHCID 7311—
ReactantAcetic AnhydrideHCID 7918—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
Solvent1,2-DichloroethaneHCID 11—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 22628567HCID 2262856792%

Reaction Steps

A mixture of 21.2 g (0.10 mol) of 2,4-di-tert-butylphenol (97%), 16.3 g (0.11 mol) of 50% aqueous glyoxylic acid and 0.05 g (0.26 mmol) of p-toluenesulfonic acid monohydrate in 30 ml of 1,2-dichloroethane is refluxed under nitrogen for 3.5 hours on a water separator. Afterwards the reaction mixture is concentrated on a vacuum rotary evaporator. The residue is taken up in 9.9 ml (0.105 mol) of acetic anhydride and the solution is refluxed for 90 minutes. The reaction mixture is then cooled to room temperature, diluted with 100 ml of tert-butyl methyl ether and washed in succession with water and dilute sodium hydrogencarbonate solution. The aqueous phases are separated and extracted with 50 ml of tert-butyl methyl ether. The organic phases are combined, dried over magnesium sulfate and concentrated on a vacuum rotary evaporator. Chromatography of the residue on silica gel with the solvent system dichloromethane/hexane=2:1 yields 28.0 g (92%) of 3-acetoxy-5,7-di-tert-butyl-3H-benzofuran-2-one (compound (206), Table 2) as a thick reddish resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607624
Source datasetuspto-grants-1997_03
ORD IDord-79462c376ef446ca80573b801b4a8886
Source noteuspto-grants-1997_03