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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865921Generated: October 27, 2026

2-Methyl-2-butene → 6-chloro-1H-indole-2,3-dicarboxylic acid 2-ethyl ester

https://huagongshe.com/reaction/1865921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantEthyl 6-chloro-3-formyl-1H-indole-2-carboxylateHCID 4591751—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product6-chloro-1H-indole-2,3-dicarboxylic acid 2-ethyl esterHCID 4512106714%

Reaction Steps

To a solution of 0.104 g (0.413 mmol) of 6-Chloro-3-formyl-1H-indole-2-carboxylic acid ethyl ester in a mixture of tert-butanol (10 ml) and H2O (5 ml), was added 2-methyl-2-butene (2 ml) followed by a solution of NaClO2 (0.344 g, 3.80 mmol) and NaH2PO4 (0.399 g, 2.90 mmol) in water (2 ml). The mixture was stirred overnight at RT. The organic solvents were removed, and then the aqueous solution diluted with water, and washed twice with hexane. The ph of the aqueous phase was adjusted to 3 by addition of aq. HCl 1N, and the product extracted with EtOAc. The combined organic phases were dried over Na2SO4 and concentrated in vacuo to afford 15 mg (14%) of 6-chloro-1H-indole-2,3-dicarboxylic acid 2-ethyl ester as alight yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629353B2
Source datasetuspto-grants-2009_12
ORD IDord-23d82c8753fe4ae6aa4c2f23c3d8a695
Source noteuspto-grants-2009_12