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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490751Generated: October 27, 2026

Indole → (5-Benzyloxy-indol-1-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/490751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantEthyl bromoacetateHCID 7748—
Reactant5-BenzyloxyindoleHCID 14624—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product(5-Benzyloxy-indol-1-yl)-acetic acid ethyl esterHCID 5989788086%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-benzyloxyindole (10.0 g, 44.79 mmol) is dissolved into anhydrous DMF (100 mL) and cooled to 0° C. in an ice water bath. Sodium hydride (2.6 g, 67.18 mmol) is dissolved into anhydrous DMF (100 mL), then slowly added to the indole solution using an addition funnel. The reaction is allowed to stir at 0° C. for 1 h., then the ice bath is removed and the solution is allowed to warm slowly to room temperature. The solution is then cooled back down to 0° C. and ethyl bromoacetate (11.2 g, 67.18 mmol) is then added in one portion. The reaction is allowed to stir at 0° C. for 1 h., then the ice bath is removed and the solution is allowed to warm slowly to room temperature. Upon completion, the reaction is quenched carefully using water, then diluted with EtOAc (300 mL). Brine (100 mL) is added and the two layers are separated in a separatory funnel. The organic layer is rinsed with water (2×75 mL) and then dried over anhydrous magnesium sulfate. The organic layer is then concentrated and purified using flash column chromatography (5% EtOAc/Hexanes) to yield 11.86 g (86%) of (5-Benzyloxy-indol-1-yl)-acetic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528160B2
Source datasetuspto-grants-2009_05
ORD IDord-ca41104a27274bf78c08b44db3705f07
Source noteuspto-grants-2009_05