HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987418Generated: October 30, 2026
Hexane → 5,6,7-Trimethoxy-2-vinylnaphthalene
https://huagongshe.com/reaction/987418
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 5,6,7-Trimethoxynaphthalene-2-carbaldehyde | HCID 21891637 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,6,7-Trimethoxy-2-vinylnaphthalene | HCID 21891570 | — |
Reaction Steps
Methyltriphenylphosphonium bromide (2.8 g) was suspended in dry THF (10 mL) under an argon atmosphere, and a 1.7 M hexane solution (3.3 mL) of tert-butyllithium was added to the suspension at −20° C. After stirring the mixture at room temperature for 1 hour, the reaction mixture was cooled again to −20° C., a solution of 5,6,7-trimethoxynaphthalene-2-carboaldehyde (1.26 g) in dry THF (30 mL) was added dropwise thereto, and the mixture was stirred overnight at room temperature. The solvent was distilled off, and water was added to the residue to conduct extraction with ethyl acetate. The resultant organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:8) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06632810B2 |
|---|
| Source dataset | uspto-grants-2003_10 |
|---|
| ORD ID | ord-b759d9f3d1be4e6c89e8bca3d96741fc |
|---|
| Source note | uspto-grants-2003_10 |
|---|