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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 551038Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/551038

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl acetateHCID 10908—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborateHCID 11375006—
Edukt4-Bromo-1-(phenylsulfonyl)-1H-indoleHCID 22015311—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkttert-Butyl [1-(phenylsulfonyl)-1H-indol-4-yl]acetateHCID 57426198—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07947677B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-4c43a41060b94d789bc27194f8068821
Quellennotizuspto-grants-2011_05