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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1159826생성일: 2026년 10월 27일

Benzylsulfonic acid → 5-(Phenylmethoxy)-1-phenylsulfonylindole

https://huagongshe.com/reaction/1159826

반응식

참여 물질

역할이름HCID투입량
반응물Benzylsulfonic acidHCID 7532—
반응물Sodium HydroxideHCID 14798—
반응물Bis(tetrabutylammonium) sulphateHCID 11433187—
반응물5-BenzyloxoindoleHCID 68714216—
용매DichloromethaneHCID 6344—
생성물5-(Phenylmethoxy)-1-phenylsulfonylindoleHCID 1182462483%

반응 단계

DCM (200 mL) was added to 5-benzyloxoindole (15 g, 67 mmol), benzylsulfonic acid (17.8 g, 101 mmol) and tetrabutyl ammoniumsulfat (6.84 g, 20 mmol) followed by 5 M NaOH (40 mL). The reaction mixture was stirred at rt for 3 h. The aqueous layer was washed with DCM (2×30 mL) and the organic layers were combined and washed with brine (30 mL). Drying (MgSO4) and concentration in vacco was followed by crystallization from MeOH to give the product in 83% yield (20.3 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07812017B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-d000031967a94d8a974ac43d6a24285f
출처 메모uspto-grants-2010_10