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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992353Generated: November 1, 2026

Benzene → Methyl 4-fluoro-1H-indole-7-carboxylate

https://huagongshe.com/reaction/992353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant4-fluoro-1H-indole-7-carboxylic AcidHCID 11579217—
SolventMethanolHCID 887—
ProductMethyl 4-fluoro-1H-indole-7-carboxylateHCID 22473012—

Reaction Steps

To a suspension of 4-fluoro-7-carboxyindole in a mixture of MeOH (18 ml)/PhH (62 ml) was added (trimethylsilyl)diazomethane (8.8 ml, 17.6 mmol, 2 M in hexane). The resulting mixture was stirred at room temperature for 30 min., quenched with excess acetic acid and evaporated in vacuo. The crude oily material was purified by flash chromatography using a gradient elution (Hexane to 10% EtOAc/Hexane) to afford methyl (4-fluoro)indole-7-carboxylate as a white solid (1.04 g, 83% two steps)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469006B1
Source datasetuspto-grants-2002_10
ORD IDord-2f8c875a55f645879ba671a1cd6d23d5
Source noteuspto-grants-2002_10