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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093463Generated: October 25, 2026

Hydrochloric Acid → 3-(Naphthalen-1-yl)propan-1-ol

https://huagongshe.com/reaction/1093463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant3-(1-Naphthalenyl)-2-propenoic acidHCID 98307—
ReactantBorane;tetrahydrofuranHCID 2723981—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-(Naphthalen-1-yl)propan-1-olHCID 14711518100%

Reaction Steps

3-(1-Naphthyl) acrylic acid (5.00 g) was dissolved in methanol (30 ml) and tetrahydrofuran (50 ml), 10% palladium carbon (2.40 g) was added, and the mixture was stirred under a hydrogen atmosphere at room temperature for 13 hr. The reaction container was purged with nitrogen, the solution was filtered, and the filtrate was concentrated to give a white solid (5.00 g. The white solid was dissolved in tetrahydrofuran (100 ml), and a tetrahydrofuran-borane.tetrahydrofuran solution (1 mol/l, 27.4 ml) was added dropwise to the mixture under ice-cooling, and the mixture was stirred under ice-cooling for 1 hr, and further at room temperature for 18 hr. To the reaction mixture was added water, 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 (4.70 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129361B2
Source datasetuspto-grants-2012_03
ORD IDord-d168bc036e1a45eaaf32c38dea6744f5
Source noteuspto-grants-2012_03