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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29337Generated: October 25, 2026

Water → Ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/29337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium percarbonateHCID 159762—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl esterHCID 68713160—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylateHCID 6871173580.6%

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-965edae8814849798c651b63a638beac
Source noteuspto-grants-2008_09