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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237353Generated: November 2, 2026

Hydrochloric Acid → Succinic mono-(2-{2-[2-(2-allyloxy-ethoxy)-ethoxy]-ethoxy}-ethyl)ester

https://huagongshe.com/reaction/2237353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantSuccinic anhydrideHCID 7922—
Reactant3,6,9,12-Tetraoxapentadec-14-en-1-olHCID 10125214—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventTolueneHCID 1140—
ProductSuccinic mono-(2-{2-[2-(2-allyloxy-ethoxy)-ethoxy]-ethoxy}-ethyl)esterHCID 86609188103.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-{2-[2-(2-allyloxy-ethoxy)-ethoxy]-ethoxy}-ethanol (9) (3.6 g, 15 mmol), succinic anhydride (1.8 g, 18 mmol), pyridine (1.22 mL, 15 mmol), dimethylaminopyridine (183 mg, 10 mol %), and dry toluene (5 mL) were charged into a screw cap culture tube. The mixture was stirred at 80° C. for 10 hours. Next, the reaction was stopped by adding 10% HCl (6 mL) and the reaction mixture was extracted with CH2Cl2 (3×10 mL). An organic layer was collected and dried on MgSO4. AMBERLITE™ resin IR-120 (+) (2 g) was added and stirred to perform ion exchange. The resin was filtered off and the filtrate was concentrated to obtain yellow oil (5.2 g, 92%). The compound was used without further purification. The NMR analysis result of the compound is as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718577B2
Source datasetuspto-grants-2010_05
ORD IDord-dad9215693bb4484abeb348fbc47530a
Source noteuspto-grants-2010_05