Resist film remover
A technology of resist film and stripper, applied in the direction of organic chemistry, photosensitive material processing, etc., can solve the problems of easy change of composition and corrosion of metal wiring, etc., and achieve the effect of excellent resist film stripping.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] The preparation of embodiment 1 chloride 1-hydroxyethyl-3-hexadecyl imidazole
[0035]Mix 1.79 g of imidazole and 3.8 mL of hexadecane bromide (the molar ratio of substances is 2:1) in 35 mL of ethyl acetate, stir for 10 minutes with magnetic force and mix well. Pour the mixture into a polytetrafluoroethylene liner with a capacity of 60mL, seal the polytetrafluoroethylene liner into a stainless steel reactor, and put it into a digital oven, heat it from room temperature to 120°C for 16 hours, and then cool it naturally to room temperature. Then the mixture was filtered to take out the filtrate, washed several times with distilled water to remove the imidazole that did not participate in the reaction, and the solvent ethyl acetate was evaporated with a rotary evaporator, and the resulting product 1-hexadecyl imidazole was dried in a vacuum oven at 70°C for 12 hours to constant weight. Obtain pale yellow liquid, weigh the product, mix 2.9g of 1-hexadecyl imidazole and 1...
Embodiment 2
[0036] Embodiment 2ω, the preparation of ω '-two (benzimidazol-2-yl) alkanes
[0037] Weigh 0.11 mol of o-phenylenediamine and 0.05 mol of fatty diacid respectively, thoroughly grind them in a mortar to make them evenly mixed, and transfer them to a three-necked flask. Add mixed acid, pass through nitrogen, and heat to reflux under mechanical stirring. TLC tracking and monitoring until the end of the reaction, about 10h, pour it into a 250mL beaker, let it stand for cooling, and adjust the pH=7 with concentrated ammonia water. Stand overnight at 4°C, filter and dry with suction, and recrystallize the crude product with methanol / water to obtain a pure product.
Embodiment 3
[0039] With N-ethyl ethyl carbamate 25g, ethylene glycol monobutyl ether 8g, gallic acid 4g, organic solvent and the chloride 1-hydroxyethyl-3-hexadecylimidazole 4g that embodiment 1 prepares, embodiment 2. Mix and stir 4 g of the prepared ω,ω′-bis(benzimidazol-2-yl)alkane until clear to obtain a release agent.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 