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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418757Generated: October 29, 2026

Benzyl Alcohol → HCID 59706550, compound

https://huagongshe.com/reaction/418757

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 acetate1:1→1:3) to give 1.69 g of the title compound as oil (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093294B2
Source datasetuspto-grants-2012_01
ORD IDord-5af85d1e3534405d97cd706d5a1cafa7
Source noteuspto-grants-2012_01