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HRID 325025作成日:2026年10月26日

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

https://huagongshe.com/reaction/325025

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物tert-butyl N-(3-hydroxyphenyl)carbamateHCID 312485—
反応物4-(2-Hydroxyethyl)benzonitrileHCID 2800815—
反応物Diethyl azodicarboxylateHCID 5462977—
溶媒TetrahydrofuranHCID 8028—
生成物t-Butyloxycarbonylamino-3-[2-(4-cyanophenyl)ethoxy]benzeneHCID 2203352244.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06221898B1
出典データセットuspto-grants-2001_04
ORD IDord-e5b8a547495d4d43b883be3cf3eaf95f
出典メモuspto-grants-2001_04