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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480365Generated: October 29, 2026

Methyl 5-(3-((tert-butoxycarbonyl)amino)prop-1-yn-1-yl)furan-2-carboxylate → 5-(3-Tert-butoxycarbonylaminopropyl)-furan-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/480365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(3-((tert-butoxycarbonyl)amino)prop-1-yn-1-yl)furan-2-carboxylateHCID 53793873—
Reactant5-(3-Tert-butoxycarbonylaminopropyl)-tetrahydrofuran-2-carboxylic acid methyl esterHCID 54235159—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-(3-Tert-butoxycarbonylaminopropyl)-furan-2-carboxylic acid methyl esterHCID 53648661—

Reaction Steps

5-(3-tert-Butoxycarbonylamino-propyl)-tetrahydrofuran-2-carboxylic acid methyl ester and 5-(3-tert-Butoxycarbonylamino-proDyl)-furan-2-carboxylic acid methyl ester. To a solution of 5-(3-tert-butoxycarbonylamino-prop-1-ynyl)-furan-2-carboxylic acid methyl ester (1.69 g) in MeOH (50 mL) was added 10% palladium on carbon (850 mg) and the mixture was hydrogenated on a Parr shaker at 50 psi for 18 h. The catalyst was removed via filtration through Celite and the volatiles were concentrated in vacuo. Flash chromatography (hexanes:EtOAc 4:1) provided 5-(3-tert-butoxycarbonylamino- propyl)-furan-2-carboxylic acid methyl ester (422 mg, MS 284 M+) followed by 5-(3-tert-butoxycarbonylamino-propyl)-tetrahydrofuran-2-carboxylic acid methyl ester (903 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649657B2
Source datasetuspto-grants-2003_11
ORD IDord-28405d54c5e64ceb8f9ecd07b0c31478
Source noteuspto-grants-2003_11