HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186255Generated: October 29, 2026
Sodium Hydroxide → 4,7-Di-t-butyl-5-hydroxy-2,3-dihydrobenzofuran
https://huagongshe.com/reaction/2186255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methanesulfonate | HCID 85257 | — |
| Reactant | 4-Tert-butyl-2,3-dihydro-5-benzofuranol | HCID 14484957 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4,7-Di-t-butyl-5-hydroxy-2,3-dihydrobenzofuran | HCID 12094549 | 97% |
Reaction Steps
In a solution of 2.84 g of 4-t-butyl-5-hydroxy-2,3-dihydrobenzofuran [J. Org. Chem. 53, 4135 (1988)] in 10.0 g of t-butyl alcohol and 20 ml of chloroform was added dropwise 10 ml of methane sulfonate under ice-cooling. The mixture was stirred at 0° C. for 15 minutes, then poured into ice water. Then, the mixture was neutralized with a 1N aqueous sodium hydroxide solution and extracted with ethyl acetate. The extracted layers were washed with a saturated aqueous sodium bicarbonate solution, dried over anhydrous magnesium sulfate and then concentrated. The concentrate was purified by silica gel column chromatography (in n-hexane) to give 1.78 g of 4,7-di-t-butyl-5-hydroxy-2,3-dihydrobenzofuran as a white crystal (yield 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403639B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-07df497ec3c54dd5864d6559dae14e0d |
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| Source note | uspto-grants-2002_06 |
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