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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108320Generated: October 30, 2026

Trifluoroacetic acid → 4-(4-Bromo-7-methoxybenzofuran-2-ylmethoxy)-piperidine

https://huagongshe.com/reaction/1108320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(4-Bromo-7-methoxybenzofuran-2-ylmethoxy)-piperidine-1-carboxylic Acid tert-butyl EsterHCID 54077020—
SolventDichloromethaneHCID 6344—
Product4-(4-Bromo-7-methoxybenzofuran-2-ylmethoxy)-piperidineHCID 1878486997.6%

Reaction Steps

Trifluoroacetic acid (5 ml) was added to a stirred solution of 4-(4-bromo-7-methoxybenzofuran-2-ylmethoxy)-piperidine-1-carboxylic acid tert-butyl ester (1.3 g) in dichloromethane (50 ml). After stirring at room temperate overnight the reaction was diluted with dichloromethane (150 ml) washed with 1M sodium hydroxide (100 ml) and dried over magnesium sulfate. The organic phase was concentrated in vacuo to afford the title compound as a pale yellow gum (0.98 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066657
Source datasetuspto-grants-2000_05
ORD IDord-ce50eecc609e43c3b6455bd48d38dc13
Source noteuspto-grants-2000_05