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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037930Generated: November 2, 2026

Water → 2-Tert-butyl-6-fluoro-5-nitro-1H-indole

https://huagongshe.com/reaction/2037930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantN-(2-(3,3-dimethylbut-1-ynyl)-5-fluoro-4-nitrophenyl)butyramideHCID 59129414—
SolventDimethylformamideHCID 6228—
Product2-Tert-butyl-6-fluoro-5-nitro-1H-indoleHCID 5342118665%

Reaction Steps

A solution of N-(2-(3,3-dimethylbut-1-ynyl)-5-fluoro-4-nitrophenyl)butyramide (3.0 g, 9.8 mmol) and TBAF (4.5 g, 17.2 mmol) in DMF (25 mL) was heated at 100° C. overnight. The mixture was poured into water and then extracted with EtOAc (80 mL×3). The combined extracts were washed with water (50 mL) and brine (50 mL), dried over Na2SO4 and concentrated under reduced pressure to dryness. The residue was purified by column chromatography on silica gel (petroleum ether/ethyl acetate 20:1) to give compound 2-tert-butyl-6-fluoro-5-nitro-1H-indole (1.5 g, 65%). 1H-NMR (400 MHz, CDCl3) δ 8.30 (d, J=7.2 Hz, 1H), 7.12 (d, J=11.6 Hz, 1H), 6.35 (d, J=1.2 Hz, 1H), 1.40 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575209B2
Source datasetuspto-grants-2013_11
ORD IDord-0b710ecd235a46dc9584ff0970dfb97b
Source noteuspto-grants-2013_11