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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212548Generated: October 26, 2026

Sodium Hydroxide → 5-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-ol

https://huagongshe.com/reaction/2212548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-indole-1-carboxylic acid tert-butyl esterHCID 69514940—
SolventEthanolHCID 702—
Product5-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-olHCID 21966601843.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 950 mg (0.3 mmol) 6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-indole-1-carboxylic acid tert-butyl ester in 20 ml EtOH was treated with 2 ml of saturated aqeous NaOH and stirred during 2 hours at 60° C. 75% of the solvent were evaporated, the resulting mixture was poured into 5 ml of water, acidified with 2M aqueous HCl, and extracted with EtOAc. Drying of the combined organic layers with MgSO4, evaporation of the solvent, and chromatography on silica gel with CH2Cl2 gave 550 mg (84%) of 5-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-ol as a viscous light yellow oil, MS: 218 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07102007B2
Source datasetuspto-grants-2006_09
ORD IDord-ba7b9d8b0040448e85904e4b0125ec39
Source noteuspto-grants-2006_09