HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3,4-Dihydro-2-hydroxy-3-(2-propenyl)-naphthalenecarboxylic Acid, Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 3,4-Dihydro-2-hydroxynaphthalenecarboxylic Acid, Methyl Ester | HCID 54692164 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-Dihydro-2-hydroxy-3-(2-propenyl)-naphthalenecarboxylic Acid, Methyl Ester | HCID 54680830 | 106.6% |
Reaction Steps
To a stirred solution of 3,4-dihydro-2-hydroxynaphthalene carboxylic acid, methyl ester (36.2 g, 177 mmol) in dry tetrahydrofuran (440 ml) at -30° C. under argon was added dropwise lithium diisopropylamide (195 ml, 2M solution, 390 mmol). Allyl bromide (24.3 ml, 284 mmol) was then added at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 1 h, then treated with hydrochloric acid (5M) to pH2-3. The resulting mixture was extracted with ethyl acetate (2×1000 ml) and the combined extracts were washed with brine (1000 ml), dried (Na2SO4) and evaporated in vacuo to give the title compound as a brown oil (46.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080752 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-a0c087aa6d9d4450b206d577f088f4f1 |
| Source note | uspto-grants-2000_06 |