HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278471Generated: October 26, 2026
1-Iodonaphthalene → Methyl 4-(1-naphthyl)-2-oxobutyrate
https://huagongshe.com/reaction/278471
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Iodonaphthalene | HCID 7004 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Methyl 2-hydroxybut-3-enoate | HCID 545123 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-(1-naphthyl)-2-oxobutyrate | HCID 18370780 | 6.9% |
Reaction Steps
To a stirred solution of Pd(OAc)2 (340 mg), nBu3P (613 mg), and Et3N (1.99 g) in DMF (30 ml) was added methyl 2-hydroxy-3-butenoate (1.76 g) followed by 1-iodonaphthalene (5.0 g), and the reaction mixture was stirred at 100° C. for 2.5 hours. The reaction mixture was poured into water (300 ml) and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel (130 g) column chromatography eluting with hexane/ethyl acetate (50:1) to give methyl 4-(1-naphthyl)-2-oxobutyrate (254 mg) as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06359145B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-9e3c425c714a4a85a45538e47de2e0fe |
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| Source note | uspto-grants-2002_03 |
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