Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 4-Hydroxyfuran-2(3H)-one | HCID 22172809 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18406868 | HCID 18406868 | 7.4% |
Reaction Steps
To 4-hydroxy-2-furanone (50 g, 0.5 mol) in tert-butanol (50 ml, 0.53 mol) was added concentrated sulfuric acid (25 ml). The mixture was heated at 40° C. for 20 h then allowed to cool. Water (250 ml) was added and the mixture was extracted with diethyl ether (3×250 ml), the diethyl ether layers were combined, washed with brine (250 ml), dried (Na2SO4), filtered and concentrated in vacuo to give a brown solid. The solid was purified by silica gel chromatography with 0%→100% ethyl acetate/isohexane as eluent followed by two recrystallisations from ethyl acetate/isohexane (1:1) to afford the required product (5.75 g). Data for the title compound: 1H NMR (400 MHz, DMSO) δ 1.21 (9H, s), 4.48 (2H, s), 11.40 (1H, s); MS (ES+) m/e 156 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476030B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-d8fc069aa3d845b5aa2229d29154ee54 |
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| Source note | uspto-grants-2002_11 |
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