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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325025생성일: 2026년 10월 25일

Triphenylphosphine → t-Butyloxycarbonylamino-3-[2-(4-cyanophenyl)ethoxy]benzene

https://huagongshe.com/reaction/325025

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물tert-butyl N-(3-hydroxyphenyl)carbamateHCID 312485—
반응물4-(2-Hydroxyethyl)benzonitrileHCID 2800815—
반응물Diethyl azodicarboxylateHCID 5462977—
용매TetrahydrofuranHCID 8028—
생성물t-Butyloxycarbonylamino-3-[2-(4-cyanophenyl)ethoxy]benzeneHCID 2203352244.3%

반응 단계

To a solution of t-butyloxycarbonylamino-3-hydroxybenzene (418.5 mg; 2 mmol; from step (i) above), triphenylphosphine (629.5 mg; 2.4 mmol) and 2-(4-cyanophenyl)ethanol (353.2 mg; 2.4 mmol) in THF (50 mL), under an atmosphere of nitrogen, was added diethylazodicarboxylate (518 mg; 3 mmol) and the mixture was stirred for one week. Ice cold water was added and the THF was removed by evaporation. The remaining water phase was extracted three times with EtOAc. The combined organic phase was washed twice with 0.2 M NaOH, once with brine, and then dried (Na2SO4). Evaporation followed by flash chromatography using a stepwise gradient of toluene:EtOAc (100:0, 90:10, 80:20 and 60:40) gave 300 mg (44%) of the sub-title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06221898B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-e5b8a547495d4d43b883be3cf3eaf95f
출처 메모uspto-grants-2001_04