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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749973Generated: November 1, 2026

Tert-butyl 4-[(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)ethynyl]piperidine-1-carboxylate → Tert-butyl 4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)ethyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/1749973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-[(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)ethynyl]piperidine-1-carboxylateHCID 71278779—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTert-butyl 4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)ethyl]piperidine-1-carboxylateHCID 7127893581.4%

Reaction Steps

A solution of tert-butyl 4-[(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)-ethynyl]piperidine-1-carboxylate (0.0721 g, 0.194 mmol) synthesized in Example B55, Step 1 in ethanol (3 mL) was added with 5% palladium/carbon (wetted with 50% water, 0.0700 g), and the mixture was stirred overnight at room temperature under a hydrogen atmosphere. The reaction mixture was filtered through Celite, and the resulting filtrate was concentrated to obtain tert-butyl 4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)ethyl]piperidine-1-carboxylate (0.0593 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-26d36988725e4d1dbbb1285d158ddc22
Source noteuspto-grants-2015_10