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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303523Generated: November 1, 2026

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

https://huagongshe.com/reaction/2303523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant1H-Indol-5-ol, 1-(phenylmethyl)-HCID 10775462—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
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 with water and extracted with 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/hexaneØ50% ether/hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433001B1
Source datasetuspto-grants-2002_08
ORD IDord-5800338a33c44a209ebcf27e5f7e0c8c
Source noteuspto-grants-2002_08