HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027338Generated: October 28, 2026
Vinyl ether → Propylene glycol methyl ether acetate
https://huagongshe.com/reaction/1027338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vinyl ether | HCID 8024 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Reactant | (2-(Ethenyloxy)ethyl)cyclohexane | HCID 21363356 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Propylene glycol methyl ether acetate | HCID 7946 | — |
Reaction Steps
Subsequently, 5.78 g of 2-cyclohexylethyl vinyl ether as the vinyl ether compound and 1.45 g of 2% camphorsulfonic acid (PGMEA solution) were added to Solution p-1, and the mixture was stirred at room temperature for 4 hours. After 1.05 g of 6% triethylamine (PGMEA solution) was added and the mixture was stirred for a while, the reaction solution was transferred to a separating funnel containing 165 mL of ethyl acetate, and the organic layer was washed with 200 mL of distilled water three times. The organic layer was concentrated by an evaporator to remove ethyl acetate, and this reaction solution was added dropwise in 2 L of hexane. A part of the obtained precipitate was sampled for NMR measurement, and the remaining was dissolved in 70 g of PGMEA. From the obtained solution, the low boiling point solvent was removed by an evaporator to obtain 105.6 g of a PGMEA solution (32.7 mass %) of Resin (P-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735048B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-bb899b5cbbc1404aa193ad517148a9b5 |
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| Source note | uspto-grants-2014_05 |
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