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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323702Generated: October 25, 2026

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

https://huagongshe.com/reaction/323702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl bromoacetateHCID 60984—
Reactant1-Benzyl-2-ethyl-1H-indol-4-OLHCID 9816416—
Product(1-Benzyl-2-ethyl-1H-indol-4-yloxy)-acetic acid methyl esterHCID 1068737169%

Reaction Steps

Using the procedure described in Example 1, Part E, in EP Publication No. 0 675 110, 2-ethyl-4-hydroxy-1-(phenylmethyl)-1H-indole (1.56 g, 6.2 mmol) was treated with 248 mg (6.2 mmol) of 60% NaH/mineral oil and then 0.6 mL (6.2 mmol) of methyl bromoacetate. The product was purified by chromatography over silica gel eluting with 20% EtOAc/hexane, to give 1.37 g (69% yield) of [[2-ethyl-1-(phenylmethyl)-1H-indol-4-yl]oxyl]acetic acid methyl ester; mp 89-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214855B1
Source datasetuspto-grants-2001_04
ORD IDord-9b76f4e8300747e7a5f0afc07b641bf8
Source noteuspto-grants-2001_04