Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Ethyl 2,3-epoxybutyrate | HCID 29774 | — |
| Product | HCID 19801420 | HCID 19801420 | — |
Reaction Steps
That is, to ethyl 2,3-epoxybutanoate (13.0 g, 0.1 mol) dissolved in isopropanol (30 ml) was added sulfuric acid (0.5 ml), and the mixture was stirred at 60° C. for 5 hours. Subsequently, excessive isopropanol was removed under reduced pressure to obtain ethyl 3-(isopropoxy)-2-hydroxybutanoate. The product obtained and p-toluenesulfonyl chloride (20.9 g, 0.11 mol) were added to pyridine (50 ml), and the mixture was stirred at room temperature for 5 hours. Subsequently, water was added to the reaction mixture, and the oily product liberated was extracted with toluene. After the toluene layer was washed with water and dried over sodium sulfate, toluene was removed under reduced pressure. The oily product obtained was isolated by silica gel column chromatography (Wako gel C-200 (trade name, produced by Wako Junyaku K.K.), eluted by hexane: ethyl acetate=9:1) to obtain ethyl 3-(isopropoxy)-2-p-toluenesulfonyloxybutanoate (27.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05178663 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-be782ff886fb4b4fb41670fd2a91ca0b |
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| Source note | uspto-grants-1993_01 |
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