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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027346Generated: October 29, 2026

Ethyl Acetate → Propylene glycol methyl ether acetate

https://huagongshe.com/reaction/1027346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-EthynylphenolHCID 32758—
CatalystSodium IodideHCID 5238—
Catalyst1-ChloromethylnaphthaleneHCID 6845—
SolventAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductPropylene glycol methyl ether acetateHCID 7946—

Reaction Conditions

Temperature70 °C

Reaction Steps

30 g of poly(p-hydroxystyrene) (VP8000) produced by Nippon Soda Co., Ltd. was dissolved in 120 mL of dimethylsulfoxide (DMSO), and 2.21 g of 1-chloromethylnaphthalene, 34.51 g of potassium carbonate and 0.56 g of sodium iodide were added thereto. The mixture was stirred at 70° C. for 4 hours, and the reaction solution was returned to room temperature. Thereafter, 100 mL of ethyl acetate and 100 mL of distilled water were added thereto, and 130 g of an aqueous 23% acetic acid solution was little by little added to the reaction solution while stirring the reaction solution in ice water. The reaction solution was transferred to a separating funnel, and 100 mL of ethyl acetate and 100 mL of distilled water were further added. After stirring, the aqueous layer was removed, and the organic layer was washed with 200 mL of distilled water five times. The organic layer was then concentrated and dissolved in 120 g of tetrahydrofuran (THF). Thereto, 26.53 g of triethylamine was added, and the reaction solution was cooled to 0° C. Furthermore, 23.43 g of the 3-chloro-3-benzyloxypropionitrile solution above was added dropwise, and the reaction solution was returned to room temperature and then stirred for 4 hours. After adding 200 ml of distilled water to the reaction solution, THF was removed by an evaporator, and 200 mL of ethyl acetate was added to the residue. The reaction solution was transferred to a separating funnel, and the aqueous layer was removed. The organic layer was washed with 200 ml of distilled water three times, concentrated to about 150 mL by an evaporator and added dropwise in 2 L of hexane. A part of the obtained precipitate was sampled for NMR measurement, and the remaining was dissolved in 75 g of PGMEA. From the obtained solution, the low boiling point solvent was removed by an evaporator to obtain 105.2 g of a PGMEA solution (29.6 mass %) of Resin (P-22).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735048B2
Source datasetuspto-grants-2014_05
ORD IDord-c9be835da54b4c9387a0badb38c4dc0f
Source noteuspto-grants-2014_05