Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906115Generated: October 30, 2026

Water → 4-(tert-butoxycarbonyl)-1H-indole-7-carboxylic acid

https://huagongshe.com/reaction/906115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantTetrahydrofuranHCID 8028—
Reactant4-tert-butyl 7-methyl 1H-indole-4,7-dicarboxylateHCID 67404014—
SolventMethanolHCID 887—
Product4-(tert-butoxycarbonyl)-1H-indole-7-carboxylic acidHCID 6740315067%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 4-tert-butyl 7-methyl 1H-indole-4,7-dicarboxylate (0.58 g, 2.10 mmol) in a mixture of methanol (20 mL), terahydrofuran (10 mL) and water (10 mL) was added a 2M aqueous solution of lithium hydroxide (2.1 mL, 4.20 mmol), and the reaction mixture was stirred at 40° C. until full consumption of starting material. The organic portion of the solvent was evaporated and the pH of the aqueous solution was adjusted to 3-4 by the addition of 1 M aqueous hydrochloric acid. The acidic aqueous phase was partitioned with ethyl acetate (150 mL), and the organic layer was separated and washed with brine, dried over sodium sulfate, filtered and concentrated to give 4-(tert-butoxycarbonyl)-1H-indole-7-carboxylic acid (0.36 g, 67%). MS (EI) for C14H15NO4: 260 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-d7d6b15f56a443b0917ed75157ae86a5
Source noteuspto-grants-2011_09