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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696374Generated: October 31, 2026

Tetrabutylammonium Fluoride → tert-Butyl [3-nitro-1H-indol-4-yl]acetate

https://huagongshe.com/reaction/1696374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactanttert-Butyl [3-nitro-1-(phenylsulfonyl)-1H-indol-4-yl]acetateHCID 57426199—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl [3-nitro-1H-indol-4-yl]acetateHCID 57426200—

Reaction Steps

To a solution of tert-butyl [3-nitro-1-(phenylsulfonyl)-1H-indol-4-yl]acetate from Step C (730 mg, 1.75 mmol) in THF (5 mL) was added tetrabutylammonium fluoride (1.0 M in THF, 5.25 mL, 5.25 mmol) and the reaction mixture was stirred at ambient temperature for 10 min, then concentrated in vacuo. The residue was partitioned between saturated aqueous NaHCO3 (5 mL) and extracted with CHCl3 (15 mL). The organic extract was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CHCl3:EtOAc—90:10 to 50:50, to give the title compound. MS: m/z=221 (M-C4H7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163752B2
Source datasetuspto-grants-2012_04
ORD IDord-8bb0e83b321f43fc983a66bf3fffcf76
Source noteuspto-grants-2012_04