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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518262Generated: November 3, 2026

Tetrabutylammonium Fluoride → Methyl 3-cyclohexyl-2-[2-(hydroxymethyl)-4-methoxyphenyl]-1-prop-2-yn-1-yl-1H-indole-6-carboxylate

https://huagongshe.com/reaction/1518262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86637862HCID 86637862—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-cyclohexyl-2-[2-(hydroxymethyl)-4-methoxyphenyl]-1-prop-2-yn-1-yl-1H-indole-6-carboxylateHCID 8663786364%

Reaction Conditions

Temperature0 °C

Reaction Steps

Tetrabutylammonium fluoride (1.3 eq., 1M solution in THF) was added dropwise to an ice cooled solution of methyl 3-cyclohexyl-2-(4-methoxy-2-{[(triisopropylsilyl)oxy]methyl}phenyl)-1-prop-2-yn-1-yl-1H-indole-6-carboxylate in THF (0.036M). The mixture was stirred at 0° C. for 1 h then diluted with EtOAc, washed with saturated aq. NH4Cl, water and brine. The organic phase was dried over Na2SO4 and evaporated in vacuo. The residual material was subjected to flash chromatography (PE:EtOAc, 3:1). After evaporation of the solvent the product was obtained as white solid (64%). MS (ES+): 432.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232390B2
Source datasetuspto-grants-2012_07
ORD IDord-113387404cd845a4a2130d12b5810501
Source noteuspto-grants-2012_07