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HRID 278511생성일: 2026년 10월 26일

Pentamethylbenzene → 5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-one

https://huagongshe.com/reaction/278511

반응식

참여 물질

역할이름HCID투입량
반응물PentamethylbenzeneHCID 12784—
반응물Tin tetrachlorideHCID 24287—
반응물5,7-Di-tert-butyl-3-hydroxy-2-benzofuranoneHCID 6850821—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-oneHCID 1091619689.3%

반응 단계

11.5 g (77.5 mmol) of pentamethylbenzene and 10 ml (85.0 mmol) of tin tetrachloride are added to a solution of 19.7 g (75.0 mmol) of 5,7-di-tert-butyl-3-hydroxy-3H-benzofuran-2-one (compound (201), Table 2, Example la) in 50 ml of 1,2-dichloroethane and the reaction mixture is refluxed for 1 hour. The reaction mixture is diluted with water and extracted three times with toluene. The organic phases are combined, washed with water, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. Crystallisation of the residue from ethanol yields 26.3 g (89%) of 5,7-di-tert-butyl-3-(2,3,4,5,6-pentamethylphenyl)-3H-benzofuran-2-one, m.p. 185-190° C. (compound (111), Table 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06359148B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-d2f17aff12324320af64444ee601ac30
출처 메모uspto-grants-2002_03