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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774398Generated: November 1, 2026

Benzyl Alcohol → HCID 59706550, compound

https://huagongshe.com/reaction/1774398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-(Pyridin-3-yl)propanoic acid--hydrogen chloride (1/1)HCID 66648902—
SolventEthyl AcetateHCID 8857—
ProductHCID 59706550HCID 5970655070%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a suspension of 3-(3-pyridyl)propionic acid hydrochloride (1.51 g, 10.0 mmol) in benzyl alcohol (3.1 mL, 30 mmol) was added p-toluenesulfonic acid monohydrate (181.8 mg, 0.96 mmol), and the mixture was stirred at 130° C. for 20 h. The reaction mixture was diluted with ethyl acetate and a saturated aqueous sodium hydrogen carbonate solution was added to separate the phases. The aqueous layer was extracted again with ethyl acetate, and the combined organic layer was concentrated with reduced pressure. The residue was subjected to silica gel column chromatography (hexane-ethyl acetate 1:1→1:3) to give 1.69 g of the title compound as oil (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260375B2
Source datasetuspto-grants-2016_02
ORD IDord-3eabb1e45c7f46d7a7a87b4df6f53e7c
Source noteuspto-grants-2016_02