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HRID 1094110作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl acetateHCID 10908—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborateHCID 11375006—
反応物4-Bromo-1-(phenylsulfonyl)-1H-indoleHCID 22015311—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物tert-Butyl [1-(phenylsulfonyl)-1H-indol-4-yl]acetateHCID 57426198—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08133891B2
出典データセットuspto-grants-2012_03
ORD IDord-2e1587af39ff4af1999cdfdc5f2eaadb
出典メモuspto-grants-2012_03