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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212549Generated: October 31, 2026

Water → 5-(6-Fluoro-2,3-dihydro-1H-indol-5-yl)-pent-4-yn-1-ol

https://huagongshe.com/reaction/2212549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-olHCID 21966601—
SolventTrifluoroacetic acid acetateHCID 23437676—
Product5-(6-Fluoro-2,3-dihydro-1H-indol-5-yl)-pent-4-yn-1-olHCID 2196661573%

Reaction Steps

A solution of 109 mg (0.5 mmol) 5-(6-Fluoro-1H-indol-5-yl)-pent-4-yn-1-ol in 3 ml AcOH/TFA 2:1 was cooled to 0° C., treated with NaCNBH3 and stirred for 1 hour at room temperature. The mixture was poured into icy water, made strongly alkaline by the addition of 2M NaOH, and extracted with EtOAc. Drying of the combined organic layers with MgSO4, evaporation of the solvent, and chromatography on silica gel with CH2Cl2/MeOH 49:1 gave 80 mg (73%) of 5-(6-Fluoro-2,3-dihydro-1H-indol-5-yl)-pent-4-yn-1-ol as a colorless oil, MS: 220 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07102007B2
Source datasetuspto-grants-2006_09
ORD IDord-795f799e963649cbbcc9cad7abd9fe03
Source noteuspto-grants-2006_09