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HRID 974729생성일: 2026년 10월 24일

Benzene → 5,7-Bis(1,1-dimethylethyl)-3-phenyl-(3H)-benzofuran-2-one

https://huagongshe.com/ko/reaction/974729

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물Hydrochloric AcidHCID 313—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물5,7-Di-tert-butyl-3-hydroxy-2-benzofuranoneHCID 6850821—
용매WaterHCID 962—
생성물5,7-Bis(1,1-dimethylethyl)-3-phenyl-(3H)-benzofuran-2-oneHCID 645535664%

반응 단계

73.3 g (0.55 mol) of ground aluminium trichloride are added over 25 minutes to a solution of 131.2 g (0.50 mol) of 5,7-di-tert-butyl-3-hydroxy-3H-benzofuran-2-one (compound (201), Table 2, Example 1a) in 250 ml (2.82 mol) of benzene and the reaction mixture is heated for 1.5 hours to reflux temperature and then refluxed for 1.5 hours. The reaction mixture is cooled to room temperature and then, cautiously with cooling, 200 ml of water are added, followed by the addition of concentrated hydrochloric acid until a homogeneous two-phase mixture forms. The organic phase is separated, washed with water, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. Crystallisation of the residue from ethanol yields 97.8 g (64%) of 5,7-di-tert-butyl-3-phenyl-3H-benzofuran-2-one, m.p. 116°-119° C. (compound (108), Table 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05607624
출처 데이터셋uspto-grants-1997_03
ORD IDord-bc04b285dcab43c4ba34a66dff0845d8
출처 메모uspto-grants-1997_03