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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460579Generated: October 27, 2026

Hydrochloric Acid → 4-(benzyloxy)-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/460579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 4-(phenylmethoxy)-1H-indole-2-carboxylateHCID 119707—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product4-(benzyloxy)-1H-indole-2-carboxylic acidHCID 273549799.4%

Reaction Steps

Ethyl 4-benzyloxyindol-2-carboxylate (10 g) was dissolved in a mixed solvent (200 ml) of dioxane-water (1:1) and potassium hydroxide (3.8 g) was added. The mixture was refluxed under heating for 2 hr. The reaction mixture was poured into ice water, made acidic with hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 4-benzyloxyindol-2-carboxylic acid as pale-yellow crystals (9.0 g). The crystals were dissolved in dimethylformamide (100 ml) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC, 7.6 g), 1-hydroxybenzotriazole hydrochloride (HOBt, 6.9 g), triethylamine (7.0 ml) and acetohydrazine (2.6 g) were added thereto. The mixture was stirred at room temperature for 6 hr. The reaction mixture was poured into ice water and the precipitated crystals were collected by filtration to give the title compound (10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196199B2
Source datasetuspto-grants-2007_03
ORD IDord-f11dfa8309674d60886c700ca5804956
Source noteuspto-grants-2007_03