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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170849Generated: October 29, 2026

Sodium hydride → 1H-Indole-5-carboxylic acid, 1-(2-methoxyethyl)-, methyl ester

https://huagongshe.com/reaction/2170849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromoethyl methyl etherHCID 80972—
Reactantmethyl 1H-indole-5-carboxylateHCID 2737635—
SolventWaterHCID 962—
Product1H-Indole-5-carboxylic acid, 1-(2-methoxyethyl)-, methyl esterHCID 6716948450%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of methyl 1H-indole-5-carboxylate (200 mg, 1.14 mmol) and sodium hydride (60% in oil, 39 mg, 1.71 mmol) in N,N-dimethylformanide (3 mL) was added 1-bromo-2-methoxyethane (190 mg, 1.37 mmol) at room temperature. Then the mixture was stirred at 60° C. for 2 hours. The mixture was poured into water (20 mL) and extracted with ethyl acetate (20 mL). The organic layer was washed with water (20 mL) and dried over sodium sulfate. After removal of the solvent, the residue was purified by column chromatography on silica gel eluting with n-hexane/ethyl acetate (2:1) to give 132 mg (50%) of the title compound as colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051296B2
Source datasetuspto-grants-2015_06
ORD IDord-6cb6d67f4d0b4e939f6ee6e390536e4f
Source noteuspto-grants-2015_06