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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473055생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/473055

반응식

참여 물질

역할이름HCID투입량
반응물5-BromoindoleHCID 24905—
반응물Phenyl vinyl sulfoneHCID 79664—
반응물Tri-o-tolylphosphineHCID 80271—
반응물DiisopropylethylamineHCID 81531—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물(E)-5-(2-(phenylsulfonyl)vinyl)-1H-indoleHCID 1552156065%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633239B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-9381a37328dc44ff90162a3771f26bff
출처 메모uspto-grants-2014_01