참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Glyoxylic Acid | HCID 760 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | 2,4-Di-tert-butylphenol | HCID 7311 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 5,7-Di-tert-butyl-3-hydroxy-2-benzofuranone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06359148B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-9a205a11fc60443ca9b1e7920677b20e |
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| 출처 메모 | uspto-grants-2002_03 |
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