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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404740Generated: October 31, 2026

Octanoic Acid → HCID 86594669, compound

https://huagongshe.com/reaction/1404740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctanoic AcidHCID 379—
ReactantGlycerolHCID 753—
CatalystPalladiumHCID 23938—
ProductHCID 86594669HCID 8659466952%

Reaction Conditions

Temperature140 °C

Reaction Steps

A stirred autoclave was charged, at room temperature, with 66.47 g (722 mmol) of glycerol, 2.53 g (17.5 mmol) of octanoic acid, 0.25 g (10 wt %) of camphosulfonic acid and 0.39 g (1.0 mol %) of Pd/C at 5%. The autoclave was then pressurized at 50 bar of dihydrogen gas H2, and then it was heated at 140° C. for 16 h, stirring vigorously. After 16 h of reaction, the reaction mixture was brought back to room temperature. The catalyst was filtered on a MILLIPORE® filter (a membrane filter) (0.1 μm) and was rinsed with absolute ethanol. The solvents were evaporated and the organic products were extracted from the glycerol phase by extraction with CH2Cl2 (3×50 ml). The organic phase was washed with water (2×30 ml) and the CH2Cl2 was then evaporated at reduced pressure. The crude reaction product was purified on a flash silica column (eluent: cyclohexane/ethyl acetate=4:1˜1:1). 1-O-octanyl-glycerol ether was obtained at an isolated yield of 52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912365B2
Source datasetuspto-grants-2014_12
ORD IDord-0a3d439ca241475ba86e3bebfcc39be2
Source noteuspto-grants-2014_12