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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616717Generated: November 2, 2026

1-Decanol → HCID 101083223, compound

https://huagongshe.com/reaction/1616717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-DecanolHCID 8174—
ReactantTriphenylphosphineHCID 11776—
ReactantFerulic AcidHCID 445858—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventTetrahydrofuranHCID 8028—
ProductHCID 101083223HCID 10108322376.2%

Reaction Steps

n-Decanol (1.58 g, 10.0 mmol), ferulic acid (1.94 g, 10.0 mmol) and triphenylphosphine (2.88 g, 11.0 mmol) were dissolved in THF (20 ml), and DIAD (40% solution of diisopropyl azodicarboxylate in toluene, 5.56 g, 11.0 mmol) was added to the solution. The reaction mixture was stirred at room temperature for 16 hr and concentrated under reduced pressure. Ethyl acetate (100 ml) was added to the residue, and the mixture was washed with 5% aqueous citric acid solution (25 ml×3) and saturated brine (25 ml) and dried over anhydrous magnesium sulfate. Magnesium sulfate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was developed by PTLC (n-hexane:ethyl acetate=2:1), and silica gel containing the object product was stirred with ethyl acetate (100 ml) for 30 min for extraction. The silica gel was filtered off, and the filtrate was concentrated under reduced pressure to give n-decanyl ferulate (2.55 g, yield 76.2%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765809B2
Source datasetuspto-grants-2014_07
ORD IDord-3a73c54b2bcd4ee585f5a5338ab60a21
Source noteuspto-grants-2014_07