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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1618854생성일: 2026년 10월 26일

Tetrahydrofuran → 1-(t-Butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene

https://huagongshe.com/reaction/1618854

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물1,3,5-Tris(4-hydroxyphenyl)benzeneHCID 348148—
반응물Bromo-t-butylacetateHCID 21584499—
반응물Potassium tert-butoxideHCID 23665647—
생성물1-(t-Butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzeneHCID 68862158—

반응 단계

18 g of 1,3,5-tris(4-hydroxyphenyl)benzene was dissolved in 500 ml of tetrahydrofuran. 6 g of potassium t-butoxide was added and the mixture was stirred at room temperature for five minutes. After the addition of 10 g of bromo-t-butylacetate dropwise, the mixture was stirred for six hours while heating at 60° C. After evaporating tetrahydrofuran under reduced-pressure, the reaction product was extracted with 300 ml of dichloromethane, purified using a silica gel column, and dried to obtain 4.6 g of 1-(t-butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08771923B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-bc4d19b534eb4a389ecc6e4921082874
출처 메모uspto-grants-2014_07