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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459999Generated: October 29, 2026

5-(methoxycarbonyl)-1H-indole-2-carboxylic acid → 2-(tert-Butyl)5-methyl1H-indole-2,5-dicarboxylate

https://huagongshe.com/reaction/459999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(methoxycarbonyl)-1H-indole-2-carboxylic acidHCID 52987916—
SolventTolueneHCID 1140—
Solvent1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
Product2-(tert-Butyl)5-methyl1H-indole-2,5-dicarboxylateHCID 68564796—

Reaction Steps

To 13 g 1H-Indole-2,5-dicarboxylic acid 5-methyl ester in 300 ml toluene, 59 ml Di-tert-butoxymethyl-dimethyl-amine were added dropwise at 80° C. Then, the reaction mixture was heated under reflux for additional 6 h. After removal of the solvents under reduced pressure the residue was dissolved in 300 ml DCM and washed with sat. aqueous NaHCO3 solution (2×100 ml). The organic layer was dried over MgSO4 and concentrated under reduced pressure. The residue was purified by chromatography on silica gel eluting with a n-heptane/ethyl acetate gradient. The fractions containing the product were collected and concentrated under reduced pressure. Yield: 8.3 g. MS (ES+): m/e=276.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196103B2
Source datasetuspto-grants-2007_03
ORD IDord-bb10148e3fda410994757dc044c9b9a2
Source noteuspto-grants-2007_03