HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648821Generated: October 27, 2026
2-Naphthalenecarboxaldehyde → 2-(2-Methoxyvinyl) naphthalene
https://huagongshe.com/reaction/648821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthalenecarboxaldehyde | HCID 6201 | — |
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Methoxyvinyl) naphthalene | HCID 54302214 | 55.5% |
Reaction Steps
To the solution produced by reacting sodium (0.92 g) in dry ethanol (60 ml) was added methoxymethyltriphenylphosphonium chloride (15.2 g). After stirring at room temperature for 0.5 hours, 2-naphthaldehyde (5.5 g) was added and the mixture heated at reflux for 5 hours. The mixture was evaporated to dryness and extracted with boiling ether, cooled to precipitate triphenylphosphine oxide, filtered and evaporated. The residue in dichloromethane (5 ml) was passed through a column of alumina and eluted with hexane to give 2-(2-methoxyvinyl) naphthalene (3.6 g), nD20 1.6505, which was hydrolysed in dioxan (50 ml) containing 2N sulphuric acid (5 ml) at 70° for 5 hours. After adding water, the mixture was extracted with ether, and the extract washed, (saturated sodium chloride), dried, (sodium sulphate) and evaporated to give 2-naphthylacetaldehyde (3.25 g) nD20 1.6232.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04736065 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-183d2c4e0ee04d399766161a913f446f |
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| Source note | uspto-grants-1988_04 |
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