HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514111Generated: October 30, 2026
Perchloric Acid → Ethyl 2-tert-butoxy-2-(1-hydroxy-3-methylnaphthalen-2-yl)acetate
https://huagongshe.com/reaction/514111
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 2-hydroxy-2-(1-hydroxy-3-methylnaphthalen-2-yl)acetate | HCID 67126334 | — |
| Solvent | tert-Butyl acetate | HCID 10908 | — |
| Product | Ethyl 2-tert-butoxy-2-(1-hydroxy-3-methylnaphthalen-2-yl)acetate | HCID 67126272 | 75.6% |
Reaction Steps
A solution of ethyl 2-hydroxy-2-(1-hydroxy-3-methylnaphthalen-2-yl)acetate (622 mg, 2.39 mmol) in tert-butyl acetate (12 mL) was treated with 70% HClO4 (20 μL) at 23° C.). After 3 h, the reaction was added slowly over 5 min to saturated NaHCO3 (25 mL). The resulting system was extracted with DCM (3×15 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated. Hexane (10 mL) was added, and the mixture was concentrated again. The residue was dissolved in benzene. The solution was wet-loaded onto a 24 g “gold” ISCO silica gel column and purified by flash chromatography (hexane→ethyl acetate) giving the desired product (286 mg, 38% yield). 1H NMR (400 MHz, CDCl3) δ 9.00 (s, 1H), 8.26 (d, J=8.2 Hz, 1H), 7.65 (d, J=8.8 Hz, 1H), 7.44 (dd, J=8.2, 8.0 Hz, 1H), 7/39 (dd, J=8.8, 8.0 Hz, 1H), 7.17 (s, 1H), 5.52 (s, 1H), 4.25-4.06 (m, 2H), 2.59 (s, 3H), 1.33 (s, 9H), 1.20 (t, J=7.0 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102614B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-bd227591104a409e9b77a6f33a5f45e7 |
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| Source note | uspto-grants-2015_08 |
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