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HRID 545904作成日:2026年10月26日

1-(Bromomethyl)-4-(trifluoromethoxy)benzene → 1'[4-(trifluoromethoxy)benzyl]spiro[furo[2,3-f][1,3]benzodioxole-7,3'-indol]-2'(1'H)-one

https://huagongshe.com/reaction/545904

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Bromomethyl)-4-(trifluoromethoxy)benzeneHCID 142785—
反応物2-(Bromomethyl)-5-(trifluoromethyl)furanHCID 2794605—
反応物spiro[furo[2,3-f][1,3]benzodioxole-7,3'-indol]-2'(1'H)-oneHCID 53375495—
反応物5,5-dimethyl-5,6-dihydrospiro[benzo[1,2-b:5,4-b']difuran-3,3'-indol]-2'(1H)-oneHCID 59263470—
生成物1'[4-(trifluoromethoxy)benzyl]spiro[furo[2,3-f][1,3]benzodioxole-7,3'-indol]-2'(1'H)-oneHCID 59263401—

反応手順

Following the procedure described in EXAMPLE 10.21, and making non-critical variations using spiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-2′(1′H)-one to replace 5,5-dimethyl-5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-2′(1′H)-one, and 1-(bromomethyl)-4-(trifluoromethoxy)benzene to replace 2-(bromomethyl)-5-(trifluoromethyl)furan, the title compound was obtained (50%) as a white solid: mp 99-101° C.; MS (ES+) m/z 456.3 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07935721B2
出典データセットuspto-grants-2011_05
ORD IDord-730e6bdfe7594677b55060607fd396db
出典メモuspto-grants-2011_05