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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404141Generated: November 1, 2026

4-(benzyloxy)-7-bromo-5-fluoro-1H-indole → 2-(4-(benzyloxy)-7-bromo-5-fluoro-1H-indol-3-yl)acetic acid

https://huagongshe.com/reaction/1404141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(benzyloxy)-7-bromo-5-fluoro-1H-indoleHCID 58303856—
Reactant2-(4-(benzyloxy)-7-bromo-5-fluoro-1-methyl-1H-indol-3-yl)acetic acidHCID 58304036—
SolventDichloromethane methanolHCID 21226129—
Product2-(4-(benzyloxy)-7-bromo-5-fluoro-1H-indol-3-yl)acetic acidHCID 5830389758%

Reaction Steps

Following the procedure (step 3, scheme 33) used to prepare compound 33-4, compound 17-1 gave compound 34-2 in 58% yield as a yellow solid after column chromatography on silica gel eluting with dichloromethane/methanol (5:1). LRMS: calc 377.0 and found: 378.0 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912220B2
Source datasetuspto-grants-2014_12
ORD IDord-e55f0157675240cea71a03970661c355
Source noteuspto-grants-2014_12