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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254607Generated: October 28, 2026

Tetrahydrofuran → 1,1-Dimethylethyl 4,7,10,13,16,19,22-heptaoxatricosanoate

https://huagongshe.com/reaction/254607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl acrylateHCID 15458—
ReactantHCID 86587580HCID 86587580—
CatalystSodiumHCID 5360545—
Product1,1-Dimethylethyl 4,7,10,13,16,19,22-heptaoxatricosanoateHCID 5789090358%

Reaction Steps

Methyl hexaethylene glycol (1.0 g, 3.37 mmol) and tert-butyl acrylate (0.216 g, 1.69 mmol) were dissolved in dry THF (10 mL). Sodium metal 0.4 mg, 0.016 mmol) was added to the solution. After stirring for 4 h at room temperature, the reaction mixture was quenched by the addition of 1 M HCl (15 mL). The quenched reaction mixture was then extracted with CH2Cl2 (1×50 mL, 1×25 mL). The organic layer was dried (MgSO4) and concentrated. After purification by silica gel chromatography (ethyl acetate as eluent), the product was obtained as an oil (0.832 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875700B2
Source datasetuspto-grants-2011_01
ORD IDord-7e58458e8a244b18942b62ca0d89f23b
Source noteuspto-grants-2011_01