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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 278506생성일: 2026년 10월 27일

Glyoxylic Acid → 5,7-Di-tert-butyl-3-hydroxy-2-benzofuranone

https://huagongshe.com/reaction/278506

반응식

참여 물질

역할이름HCID투입량
반응물Glyoxylic AcidHCID 760—
반응물WaterHCID 962—
반응물2,4-Di-tert-butylphenolHCID 7311—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
용매1,2-DichloroethaneHCID 11—
생성물5,7-Di-tert-butyl-3-hydroxy-2-benzofuranoneHCID 6850821—

반응 단계

A mixture of 212.5 g (1.00 mol) of 2,4-di-tert-butylphenol (97%), 163.0 g (1.10 mol) of 50% aqueous glyoxylic acid and 0.5 g (2.6 mmol) of p-toluenesulfonic acid monohydrate in 300 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 800 ml of hexane and washed three times with water. The aqueous phases are separated in the separating funnel and further extracted with 300 ml of hexane. The organic phases are combined, dried over magnesium sulfate and concentrated on a vacuum rotary evaporator. The residue yields 262.3 g (˜100%) of analytically pure 5,7-di-tert-butyl-3-hydroxy-3H-benzofuran-2-one in the form of a thick yellowish resin (compound (201), Table 2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06359148B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-9a205a11fc60443ca9b1e7920677b20e
출처 메모uspto-grants-2002_03