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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517345Generated: October 30, 2026

5-[5-(Benzyloxycarbonyl)furan-2-yl]-4-tert-butoxycarbonyl-4-pentenoic acid ethyl ester → 5-[2-(Tert-butoxycarbonyl)-5-ethoxy-5-oxopentyl]furan-2-carboxylic acid

https://huagongshe.com/reaction/517345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-[5-(Benzyloxycarbonyl)furan-2-yl]-4-tert-butoxycarbonyl-4-pentenoic acid ethyl esterHCID 77934522—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-[2-(Tert-butoxycarbonyl)-5-ethoxy-5-oxopentyl]furan-2-carboxylic acidHCID 70869255—

Reaction Steps

5-[5-(Benzyloxycarbonyl)furan-2-yl]-4-tert-butoxycarbonyl-4-pentenoic acid ethyl ester obtained in step 2 was dissolved in ethanol (5 mL), a catalytic amount of 10% palladium/carbon was added, and the mixture was stirred at room temperature for 1 hour under a hydrogen atmosphere. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure to give the title compound (82 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115107B2
Source datasetuspto-grants-2015_08
ORD IDord-ad9e52d013f9432094d3a6de08a443c2
Source noteuspto-grants-2015_08