HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352407Generated: November 1, 2026
2-Acetylnaphthalene → HCID 86743478, compound
https://huagongshe.com/reaction/2352407
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Acetylnaphthalene | HCID 7122 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-((diethoxyphosphoryl)methyl)benzoate | HCID 10979490 | — |
| Catalyst | 15-Crown-5 | HCID 36336 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 86743478 | HCID 86743478 | — |
Reaction Steps
31 g of diethyl 4-ethoxycarbonyl-benzylphosphonate and a few drops of 1,4,7,10,13-pentaoxa-cyclopentadecane are added to a suspension of 5.5 g of sodium hydride in 100 cm3 of tetrahydrofuran. The mixture is stirred at 45° C. for one hour and 17 g of 2-acetyl-naphthalene are then added. It is kept at 45° C. for three hours, allowed to cool, then diluted with dichloroethane. The insoluble matter is filtered off and the filtrate is evaporated under reduced pressure. The residue is recrystallised twice from ethanol. 14 g of the expected product are obtained. Melting point: 96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04876381 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-2c73df5cc4e740548b913a7f50703d39 |
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| Source note | uspto-grants-1989_10 |
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