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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium percarbonateHCID 159762—
EduktBorane;tetrahydrofuranHCID 2723981—
Edukt3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl esterHCID 68713160—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylateHCID 6871173580,6%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420001B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-965edae8814849798c651b63a638beac
Quellennotizuspto-grants-2008_09