HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850423Generated: October 31, 2026
2-Methyl-2-butene → HCID 19363375, compound
https://huagongshe.com/reaction/850423
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19363267 | HCID 19363267 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 19363375 | HCID 19363375 | 76.5% |
Reaction Steps
1-Bromo-4-pentyloxynaphthalene-2-carbaldehyde (0.77 g, 2.4 mmol), t-butanol (4.8 ml) and 2-methyl-2-butene (1.71 ml, 16.1 mmol) were mixed, and a solution prepared by mixing sodium chlorite (360 mg, 3.12 mmol), sodium dihydrogenphosphate (374 mg, 3.12 mmol) and water (2.4 ml) was added dropwise. The mixture was stirred at room temperature for 16.5 hours. A 1N aqueous sodium hydroxide solution (5 ml) was added, and t-butanol was evaporated under reduced pressure. Conc. hydrochloric acid was added to make the mixture acidic. Saturated saturated brine (5 ml) was added, and the aqueous layer was extracted 3 times with ethyl acetate (10 ml). The organic layer was dried over anhydrous magnesium sulfate, and the drying agent was filtered off. The filtrate was concentrated under reduced pressure. The obtained residue was recrystallized from ethyl acetate to give 1-bromo-4-pentyloxynaphthalene-2-carboxylic acid (619 mg, 76%) as pale-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06017919 |
|---|
| Source dataset | uspto-grants-2000_01 |
|---|
| ORD ID | ord-eadc08ab68584531b4591fd5a629c30e |
|---|
| Source note | uspto-grants-2000_01 |
|---|