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HRID 521937作成日:2026年10月26日

Triphenylphosphine → HCID 86713875、化合物

https://huagongshe.com/reaction/521937

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物(-)-3-HydroxytetrahydrofuranHCID 641512—
反応物Methyl 2-(2,6-difluoro-4-hydroxyphenyl)thiazole-4-carboxylateHCID 136377230—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 86713875HCID 86713875—

反応手順

To a solution of methyl 2-(2,6-difluoro-4-hydroxy-phenyl)thiazole-4-carboxylate (207 mg, 0.763 mmol) and (R)-3-hydroxytetrahydrofuran (3 equiv., 206 mg) in tetrahydrofuran (5 mL) was added triphenylphosphine (3 equiv., 600 mg) and diisopropyl azodicarboxylate (3 equiv., 0.45 mL) The mixture was stirred at RT for 2 days. The mixture was concentrated and partitioned between EtOAc and water. The organic layer was washed with sat. NaHCO3, brine, dried over Na2SO4 and concentrated. This residue was diluted with THF (3 mL) and water (1 mL) and LiOH (36 mg) was added. After stirring at rt for 2.5 hours, the reaction was neutralized with 1 N HCl(aq), diluted with EtOAc and washed with brine. The organic extracts were dried (Na2SO4) and concentrated in vacuo to provide the title compound, contaminated with triphenylphosphine oxide, and other by-products, which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328106B2
出典データセットuspto-grants-2016_05
ORD IDord-ebe1ff9fcb5a4c20b9cbe9433f928802
出典メモuspto-grants-2016_05