HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792251Generated: October 25, 2026
Vinyl Acetate → Triethylene glycol monovinyl ether monoacetate
https://huagongshe.com/reaction/1792251
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | Triethylene Glycol | HCID 8172 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Ethanol, 2-(2-(2-(ethenyloxy)ethoxy)ethoxy)- | HCID 575880 | — |
| Reactant | Triethylene glycol divinyl ether | HCID 3033992 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Triethylene glycol monovinyl ether monoacetate | HCID 22034547 | — |
Reaction Steps
To a mixture of di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [Ir(cod)Cl]2 (0.01 mmol) and sodium acetate (1.2 mmol) in toluene (2.0 ml),triethylene glycol (1 mmol) and vinyl acetate (4 mmol) were added, followed by stirring at 100° C. in an atmosphere of argon gas for 6 hours. The reaction mixture was analyzed by gas chromatography to find that triethylene glycol divinyl ether, triethylene glycol monovinyl ether, and triethylene glycol monovinyl ether monoacetate were produced in yields of 63%, 3%, and 18%, respectively, with a conversion from triethylene glycol of 100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07074970B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-23d6d4ffa44348848a0b664c32a65c64 |
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| Source note | uspto-grants-2006_07 |
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