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HRID 473055作成日:2026年10月26日

5-Bromoindole → (E)-5-(2-(phenylsulfonyl)vinyl)-1H-indole

https://huagongshe.com/reaction/473055

反応式

関与物質

役割名称HCID仕込み量
反応物5-BromoindoleHCID 24905—
反応物Phenyl vinyl sulfoneHCID 79664—
反応物Tri-o-tolylphosphineHCID 80271—
反応物DiisopropylethylamineHCID 81531—
触媒palladium(II) acetateHCID 167845—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物(E)-5-(2-(phenylsulfonyl)vinyl)-1H-indoleHCID 1552156065%

反応手順

A solution of 5-bromoindole (5.0 g, 25.5 mmol), phenylvinylsulfone (7.50 g, 44.64 mmol), Pd(OAc)2 (0.46 g, 2.05 mmol), tri-O-tolylphosphine (1.55 g, 5.10 mmol) and DIPEA (3.6 g) was heated to reflux for 18 h in acetonitrile. The reaction mixture was cooled to RT, diluted with dichloromethane and filtered over a bed of filter aid. The solvent is completely distilled off and to the crude fresh dichloromethane was charged. The filtrate was sequentially washed with water and brine, and dried over sodium sulphate. The organic layer was concentrated under vacuum and the product precipitated from ethylacetate and hexane as a solid in about 65-70% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633239B2
出典データセットuspto-grants-2014_01
ORD IDord-9381a37328dc44ff90162a3771f26bff
出典メモuspto-grants-2014_01