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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1094110생성일: 2026년 10월 24일

tert-Butyl acetate → tert-Butyl [1-(phenylsulfonyl)-1H-indol-4-yl]acetate

https://huagongshe.com/ko/reaction/1094110

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl acetateHCID 10908—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborateHCID 11375006—
반응물4-Bromo-1-(phenylsulfonyl)-1H-indoleHCID 22015311—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물tert-Butyl [1-(phenylsulfonyl)-1H-indol-4-yl]acetateHCID 57426198—

반응 단계

To a mixture of 1,3-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate (94 mg, 0.196 mmol), tris(dibenzylideneacetone)dipalladium (180 mg, 0.196 mmol), and lithium bis(trimethylsilyl)amide (1.37 M in t-BuOMe, 11.0 mL, 15.1 mmol) were added 4-bromo-1-(phenylsulfonyl)-1H-indole from Step A (2.20 g, 6.54 mmol), tert-butyl acetate (988 mg, 8.51 mmol), and toluene (15 mL). The resulting mixture was stirred at ambient temperature for 18 h then partitioned between Et2O (100 mL) and saturated aqueous NH4Cl (30 mL). The organic layer was washed with brine, then dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 85:15, to give the title compound. MS: m/z=316 (M−C4H7).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08133891B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-2e1587af39ff4af1999cdfdc5f2eaadb
출처 메모uspto-grants-2012_03