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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093468Generated: November 1, 2026

Hydrochloric Acid → 3-(2,3-Dihydro-1-benzofuran-5-yl)propan-1-ol

https://huagongshe.com/reaction/1093468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant3-(2,3-Dihydro-1-benzofuran-5-yl)propanoic acidHCID 2815405—
SolventTetrahydrofuranHCID 8028—
Product3-(2,3-Dihydro-1-benzofuran-5-yl)propan-1-olHCID 53425002103%

Reaction Steps

3-(2,3-Dihydrobenzofuran-5-yl)propionic acid (2.00 g) was dissolved in tetrahydrofuran (20 ml), and a tetrahydrofuran-borane.tetrahydrofuran solution (1 mol/l, 11.5 ml) was added dropwise to the mixture under ice-cooling. The mixture was stirred under ice-cooling for 1 hr, and further at room temperature for 16 hr. Water was added to the reaction mixture, and 1M aqueous hydrochloric acid solution was added. The mixture was extracted with ethyl acetate, washed with water, saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the object product (1.91 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129361B2
Source datasetuspto-grants-2012_03
ORD IDord-92bd6c83ced041d09f489f479e3424ed
Source noteuspto-grants-2012_03