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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338320Generated: October 25, 2026

Hydrochloric Acid → 6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/338320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylateHCID 86698666—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylic acidHCID 8669866724%

Reaction Steps

A solution of methyl 6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylate (75 mg, 0.22 mmol), methanol (2.2 mL), and aqueous sodium hydroxide (1M, 0.75 mL, 0.75 mmol) was heated at 75° C. for 24 hours. The reaction was acidified with 1M HCl to pH=2 then diluted with ethyl acetate. The aqueous layer was back-extracted twice with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to provide a crude solid. The crude product was dissolved in methylene chloride and methanol and silica gel was added. The solvent was removed in vacuo and the crude material adsorbed onto silica was loaded onto a column of silica gel and eluted with ethyl acetate (with 0.2% formic acid)/heptanes (1:1 to 1:0) to provide the title compound (17 mg, 24%) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-42f33efa79e1451395cc522a2a7331af
Source noteuspto-grants-2014_11