HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581907Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 70100107, compound
https://huagongshe.com/reaction/1581907
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Vinyl isobutyl ether | HCID 7992 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1-Ethoxypropan-2-yl acetate | HCID 171378 | — |
| Product | HCID 70100107 | HCID 70100107 | — |
Reaction Steps
The above polymer (A-48) (20 g) was dissolved in 80 g of propylene glycol monoethyl ether acetate (PGMEA) and the solution was heated at 60° C., and then the pressure was gradually reduced until 20 mmHg, thereby PGMEA and the moisture in the reaction system were azeotropically hydrated. After the azeotropic hydration, the temperature was lowered to 20° C., 2.2 g of isobutyl vinyl ether was added thereto, and further 3 mg of p-toluenesulfonic acid was added. After the addition, reaction was performed for 2 hours, and a small amount of triethylamine was added to neutralize the acid. Thereafter, ethyl acetate was added to the reaction solution, and the salt was removed by washing with ion exchange water. Further, ethyl acetate and water were distilled off under reduced pressure, thereby polymer A-16 was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06733951B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-ad5e0c7567b14f32bf459e74aca1bf7e |
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| Source note | uspto-grants-2004_05 |
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