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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353240Generated: October 26, 2026

4-Bromo-2-butenoic acid → Indole-2-carboxylic acid

https://huagongshe.com/reaction/353240

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-butenoic acidHCID 84140—
Reactant2-(4-Carboxy-n-butyl)indoleHCID 18761639—
Reactant2-Methylhexanedioyl dichlorideHCID 22560979—
ProductIndole-2-carboxylic acidHCID 72899—

Reaction Steps

Refer to 32(a) using 4-bromo-2-butenoic acid as the alkylating agent. Preparation of 2-(4-carboxy-n-butyl) indole: Refer to Example 3 using methyl adipyl chloride as the acid chloride. The methyl ester was hydrolyzed in the cyclization workup to provide the product carboxyindole. In the alternative, refer to Example 32b) using 2-(4-carboxy-3-buten-1-yl) indole as the starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750240B2
Source datasetuspto-grants-2004_06
ORD IDord-8b14d6ab190d44cd99a3d23791482055
Source noteuspto-grants-2004_06