HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29337Erstellt: 23. Oktober 2026
Water → Ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylate
https://huagongshe.com/de/reaction/29337
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium percarbonate | HCID 159762 | — |
| Edukt | Borane;tetrahydrofuran | HCID 2723981 | — |
| Edukt | 3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl ester | HCID 68713160 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylate | HCID 68711735 | 80,6% |
Reaktionsschritte
To a solution of 0.35 g (1.5 mmol) of 3-methyl-4-vinyl-1-benzofuran-2-carboxylate (Example 87, Step 1) in 3 mL of THF, cooled in an ice bath, was added 1 mL (1 mmol) of borane-THF complex (1.0M solution in THF). The reaction was stirred at room temperature for 2 hours. The reaction was cooled in an ice bath and 1.5 mL of water was added. Next 0.61 g of sodium percarbonate was added in one portion. The reaction was heated at ˜50° C. for 1 hour, then cooled to room temperature. Water was added and the resulting mixture was extracted with ethyl acetate. The organic layer washed with water and brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with hexane/ethyl acetate (2:1) to provide 0.20 g of ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylate. Yield 54%. m.p. 88-90° C.; MS 249.1 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07420001B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-965edae8814849798c651b63a638beac |
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| Quellennotiz | uspto-grants-2008_09 |
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