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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908424Generated: October 27, 2026

Water → 2-tert-butyl-4-fluoro-1H-indole

https://huagongshe.com/reaction/1908424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-(2-(3,3-dimethylbut-1-ynyl)-3-fluorophenyl)butyramideHCID 59129310—
SolventDimethylformamideHCID 6228—
Product2-tert-butyl-4-fluoro-1H-indoleHCID 59129240151.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of N-(2-(3,3-dimethylbut-1-ynyl)-3-fluorophenyl)butyramide (6.0 g, 20 mmol) in DMF (100 mL) was added t-BuOK (5.0 g, 50 mmol) at room temperature. The mixture was heated at 90° C. overnight before it was poured into water and extracted with EtOAc (100 mL×3). The organic layers were washed with sat. NaCl and water, dried over anhydrous Na2SO4, and evaporated under vacuum to give 2-tert-butyl-4-fluoro-1H-indole (5.8 g, 97%). 1H NMR (400 MHz, CDCl3) δ 8.17 (br s, 1H), 7.11 (d, J=7.2 Hz, 1H), 7.05-6.99 (m, 1H), 6.76-6.71 (m, 1H), 6.34 (m, 1H), 1.41 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-e72d893eb15e41c3afd496110198fb0f
Source noteuspto-grants-2013_12