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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 965218생성일: 2026년 10월 26일

Phenol → (+/-)cis-1-(2-Benzylphenoxy)-2-tert-butoxycarbonylaminoindane

https://huagongshe.com/reaction/965218

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Diethyl EtherHCID 3283—
반응물2-BenzylphenolHCID 24216—
반응물(+/-)N-tert-butoxycarbonyl-1,2-iminoindaneHCID 53697243—
촉매Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
용매ChloroformHCID 6212—
생성물(+/-)cis-1-(2-Benzylphenoxy)-2-tert-butoxycarbonylaminoindaneHCID 1866128624.8%

반응 단계

A solution of (±) N-tert-butoxycarbonyl-1,2-iminoindane (2.33 g, 10 mmol), 2-hydroxy diphenylmethane (1.84 g, 10 mmol) and pyridinium p-toluenesulfonate (50 mg) in chloroform (100 ml) was heated at reflux for 3 h. On cooling, the solution was washed sequentially with aq. NaHCO3, water and then brine. After drying over Na2SO4, solvents were removed in vacuo and the resultant brown oil subjected to column chromatography on silica gel eluting with 10% diethyl ether in hexanes to afford a pale yellow oil which was a mixture of the desired adduct and the starting phenol. This mixture was taken up in 1:1 diethyl ether:pentane (200 ml) and washed three times with a 1:1 mixture of methanol and 10% aq. NaOH. After washing with water then brine, the organics were dried over Na2SO4 and then concentrated in vacuo. The residue was recrystallised to afford the title compound as a white solid (1.03 g) m.p. 113°-114.5° C. (from diethyl ether-pentane).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05773463
출처 데이터셋uspto-grants-1998_06
ORD IDord-6b6fd28f0b014cdc9aace03856d7fca4
출처 메모uspto-grants-1998_06