HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295539Generated: October 26, 2026
Water → 2-Ethenyl-6-(1-ethoxyethoxy)naphthalene
https://huagongshe.com/reaction/1295539
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 6-(1-Ethoxy ethoxy)-2-naphthaldehyde | HCID 23135759 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Ethenyl-6-(1-ethoxyethoxy)naphthalene | HCID 23135760 | 96.3% |
Reaction Steps
In a 1 L three neck flask, equipped with an overhead mechanical stirrer, was added 45 g of methyltriphenylphosphonium bromide (0.126 mol) under nitrogen atmosphere. To this were added anhydrous 300 mL of THF and 16.02 g of potassium tert-butoxide (0.1428 mol). After 1 h of stirring, 20 g of 6-(1-ethoxy ethoxy)-2-naphthaldehyde (0.0819 mol), dissolved in 50 mL of THF, was added dropwise using a cannular and the reaction mixture was stirred overnight. After overnight stirring, deionized water (200 mL) was added with a syringe and the phases were separated. The aqueous phase was extracted with ether (2×100 mL) and the combined extracts were dried over MgSO4. After filtration and concentration, the crude product was purified by column chromatography (silica gel, hexane/CH2Cl2 40/60˜10/90) to yield 19.12 g of pure 6-(1-ethoxy ethoxy)-2-vinylnaphthalene (96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244542B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-f4da50241bf44b99991b984e1bf7525f |
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| Source note | uspto-grants-2007_07 |
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