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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 5-(3-((tert-butoxycarbonyl)amino)prop-1-yn-1-yl)furan-2-carboxylate | HCID 53793873 | — |
| Reactant | 5-(3-Tert-butoxycarbonylaminopropyl)-tetrahydrofuran-2-carboxylic acid methyl ester | HCID 54235159 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(3-Tert-butoxycarbonylaminopropyl)-furan-2-carboxylic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06649657B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-28405d54c5e64ceb8f9ecd07b0c31478 |
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| Source note | uspto-grants-2003_11 |
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