HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425569Generated: October 31, 2026
HCID 14317723, compound → HCID 66636992, compound
https://huagongshe.com/reaction/2425569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 14317723 | HCID 14317723 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66636992 | HCID 66636992 | 88% |
Reaction Steps
A suspension of methyl triphenylphosphonium bromide (2.41 g, 6.74 mmol) in THF (20 ml) was added dropwise potassium tert-butoxide (756 mg, 6.74 mmol) in THF (20 ml) at 0° C., and the mixture was stirred at room temperature for 1.5 hours. Then, methyl 6-acetyl-2-naphthoate (J. Org. Chem., 1990, 55, 319-324, 769 mg, 3.37 mmol) in THF (5 ml) was added at room temperature, and the resulting mixture was stirred at room temperature for 2 hours. The reaction was quenched with water (100 ml) and extracted with ethyl acetate-hexane (1:2). The organic layer was dried over sodium sulfate and concentrated in vacuo. The crude material was purified by silica gel column chromatography, eluting with ethyl acetate-hexane (0:100 to 1:20) to give 0.67 g (88% yield) of the title compound as white solid. 1H NMR (270 MHz, CDCl3) δ 2.28 (3H, s), 3.99 (3H, s), 5.26 (1H, s), 5.58 (1H, s), 7.74 (1H, d, J=8.6 Hz), 7.82-7.97 (3H, m), 8.05 (1H, d, J=8.6 Hz), 8.58 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964732B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-3225ba91295742159b9f788d1a84d467 |
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| Source note | uspto-grants-2011_06 |
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