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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3339Generated: October 24, 2026

Sodium hydride → (1-Benzyl-2-methyl-1H-indol-4-yloxy)-acetic acid methyl ester

https://huagongshe.com/en/reaction/3339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl bromoacetateHCID 60984—
Reactant1-Benzyl-2-methyl-1H-indol-4-olHCID 10752360—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(1-Benzyl-2-methyl-1H-indol-4-yloxy)-acetic acid methyl esterHCID 1080481988%

Reaction Steps

4-Hydroxy-2-methyl-1-(phenylmethyl)-1H-indole (530 mg, 2.2 mmol) was added to 88 mg (2.2 mmol) of 60% NaH/mineral oil in 20 mL of DMF and the mixture stirred for 0.67 hours. Then, 0.21 mL (2.2 mmol) of methyl bromoacetate was added and stirring maintained for 17 hours. The mixture was diluted with water and extracted with ethyl acetate. The ethyl acetate solution was washed with brine, dried (MgSO4), and concentrated at reduced pressure. The residue was chromatographed on silica gel eluting with 20% EtOAc/hexane to give 597 mg (88% yield) of [[2-methyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]acetic acid methyl ester, 140°-143° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733923
Source datasetuspto-grants-1998_03
ORD IDord-19b0abee38be4025b9f496f094d7d0bd
Source noteuspto-grants-1998_03