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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581115Generated: October 27, 2026

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

https://huagongshe.com/reaction/581115

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 inmol) 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 numberUS05919810
Source datasetuspto-grants-1999_07
ORD IDord-7da1cf0cb0cf4c6dbb4d67b31fccb6f5
Source noteuspto-grants-1999_07