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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781970Generated: November 2, 2026

Ethylene Glycol → HCID 59537271, compound

https://huagongshe.com/reaction/1781970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl 3-oxododecanoateHCID 3017756—
SolventBenzeneHCID 241—
ProductHCID 59537271HCID 5953727179%

Reaction Steps

The mixture of ethyl 3-oxododecanoate (1.456 g, ca. 5 mmol), ethylene glycol (2.78 mL, 50 mmol) and a catalytic amount of p-TsOH (95 mg, 0.5 mmol) in benzene (50 mL) was heated to 110° C. under an argon atmosphere overnight. The solvent was removed, and the residue was diluted with 50 mL ethyl acetate. The solution was washed with saturated aqueous NaHCO3 (50 mL) and brine (50 mL), and the organic phase was dried over MgSO4 and concentrated. The residue was purified by flash chromatography (hexane/EtOAc 8:1, Rf=0.21) to give ethyl 3,3-ethylenedioxydodecanoate (1.131 g, 3.95 mmol) in 79% overall yield for the above two steps. 1H NMR (500 MHz, CDCl3) δ 0.88 (t, J=7 Hz, 3H), 1.20-1.44 (m, 17H), 1.76-1.82 (m, 2H), 2.65 (s, 2H), 3.94-4.04 (m, 4H), 4.16 (q, J=7 Hz, 2H); 13C NMR (125 MHz, CDCl3) δ 14.1, 22.6, 23.4, 29.22, 29.43, 29.48, 29.62, 31.8, 37.7, 42.5, 60.4, 65.0, 109.4, 169.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498292B2
Source datasetuspto-grants-2009_03
ORD IDord-bccd1606f68f46538243c62ad1d15035
Source noteuspto-grants-2009_03