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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476983Generated: October 29, 2026

Sodium Hydroxide → 1-(1-Methylethyl)-7-(methyloxy)-1H-indole-4-carboxylic acid

https://huagongshe.com/reaction/1476983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 1-(1-methylethyl)-7-(methyloxy)-1H-indole-4-carboxylateHCID 67468655—
SolventEthanolHCID 702—
Product1-(1-Methylethyl)-7-(methyloxy)-1H-indole-4-carboxylic acidHCID 6746868292.7%

Reaction Steps

Added 1 N sodium hydroxide (6.47 mL, 6.47 mmol) to a solution of methyl 1-(1-methylethyl)-7-(methyloxy)-1H-indole-4-carboxylate (400 mg, 1.618 mmol) in ethanol (30 mL) and heated at reflux for 3 h. The EtOH was removed in vacuo and the residue dissolved in 20 ml of water. Acidifed solution by addition of 1 N HCl and extracted with DCM. the combined DCM extracts were washed with water and brine, dried over MgSO4, filtered and concentrated to give 350 mg of the title compound. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.51 (d, 6H), 4.03 (s, 3H), 5.47 (dt, J=13.39, 6.69 Hz, 2H), 6.70 (d, J=8.34 Hz, 2H), 7.23 (d, J=3.28 Hz, 2H), 7.37 (d, J=3.03 Hz, 2H), 7.99 (d, J=8.34 Hz, 2H). MS(ES) [M+H]+ 234.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402836B2
Source datasetuspto-grants-2016_08
ORD IDord-fdedcacb02a74e8f8754e76a2ab66c6a
Source noteuspto-grants-2016_08