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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256264Generated: October 29, 2026

Water → 4-[[1-(phenylmethyl)-1H-indol-5-yl]oxy]butanoic acid ethyl ester

https://huagongshe.com/reaction/2256264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant1H-Indol-5-ol, 1-(phenylmethyl)-HCID 10775462—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventDiethylether hexaneHCID 21584099—
Product4-[[1-(phenylmethyl)-1H-indol-5-yl]oxy]butanoic acid ethyl esterHCID 1059303940.4%

Reaction Steps

A solution of 850 mg (4.0 mmol) of 5-hydroxy-1-(phenylmethyl)-1H-indole in 75 mL of DMF and 20 mL of THF was treated with 200 mg (5.0 mmol) of 60% NaH/mineral oil and after stirring for 0.17 hours, 0.7 mL (4.9 mmol) of ethyl 4-bromobutyrate was added. After 2.75 hours, the mixture was diluted wish water and extracted wish EtOAc. The EtOAc solution was washed with water, saturated NaCl solution, dried(Na2SO4) and concentrated at reduced pressure. The residue was chromatographed on silica gel and the 545 mg (40% yield) of 4-[[1-(phenylmethyl)-1H-indol-5-yl]oxy]butanoic acid ethyl ester by eluting with a gradient, 15% ether/hexane→50% ether/hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654326
Source datasetuspto-grants-1997_08
ORD IDord-f67106cb442349a9970a6369c07982d8
Source noteuspto-grants-1997_08