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HRID 1444330作成日:2026年10月27日

Phosphorus oxide (P4O10) → 2-(3-Bromo-phenyl)-1-(5-phenyl-furan-2-yl)-ethanone

https://huagongshe.com/reaction/1444330

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物(3-Bromophenyl)acetic acidHCID 74653—
反応物2-PhenylfuranHCID 519363—
溶媒1,2-DichlorobenzeneHCID 7239—
生成物2-(3-Bromo-phenyl)-1-(5-phenyl-furan-2-yl)-ethanoneHCID 59654728—

反応条件

温度80 °C

反応手順

2-Phenyl-furan (119) (50 mg, 0.28 mmol) and (3-bromo-phenyl)-acetic acid (134 mg, 0.63 mmol) were dissolved in ortho-dichlorobenzene (4 ml). P2O5 (202 mg, 1.42 mmol) was added as a suspension in ortho-dichlorobenzene (2 ml). The reaction mixture was heated to 80° C. for 2 h and cooled to room temperature overnight. After the addition of further P2O5 (202 mg, 1.42 mmol), heating was resumed at 90° C. for 3 h. The reaction mixture was cooled to 0° C. and quenched with H2O (15 ml). The organic layer was separated and the aqueous layer was washed with DCM (3×10 ml). The combined organic layers were dried (MgSO4), filtered and the DCM removed in vacuo. The ortho-dichlorobenzene solution was loaded to a silica-gel column and flushed with heptane (100 ml). The title compound was then eluted with 10% EtOAc in heptane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07662839B2
出典データセットuspto-grants-2010_02
ORD IDord-c3b5924588204046aff485ab80bd94be
出典メモuspto-grants-2010_02