HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491403Generated: October 31, 2026
Water → Methyl 5-(3-oxopropyl)furan-2-carboxylate
https://huagongshe.com/reaction/491403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 5-bromofuran-2-carboxylate | HCID 599633 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 5-(3-oxopropyl)furan-2-carboxylate | HCID 12412564 | 28.1% |
Reaction Steps
A solution of 5-bromo-2-furancarboxylic acid methyl ester (816 mg, MAYB) in DMF (3 ml) was added with tetra-n-butylammonium chloride (1.1 g, TCI), sodium hydrogencarbonate (688 mg), palladium acetate (10.4 mg, WAKO), and allyl alcohol (346 mg, TCI), and the mixture was stirred at 60° C. for 20 hours. The reaction solution was added with distilled water (30 ml), and ethyl acetate (20 ml), and the insoluble solid was removed by filtration. The filtrate was extracted with ethyl acetate (50 ml×2). The organic layers were combined, washed with saturated brine, and dried, and then the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (Flash, hexane:ethyl acetate=4:1) to obtain the title compound (Intermediate ih-01, 204 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07531533B2 |
|---|
| Source dataset | uspto-grants-2009_05 |
|---|
| ORD ID | ord-9400ccdb69da490ba630e83494046cda |
|---|
| Source note | uspto-grants-2009_05 |
|---|