Degradable photoresist resin monomer synthesized from oxaspiro [4.5] decane diketone and synthesis method thereof
A technology of resin monomer and decanedione, applied in the field of resin monomer and its synthesis, can solve the problems of insufficient resolution, weak etching resistance, etc. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0026]
[0027] The first step: a, preparation of methyl Grignard reagent: adding magnesium chips (2.9g, 119mmol) in anhydrous ether (15mL), then adding an iodine tablet, then adding methyl bromide (11.3g, 119mmol) Dissolve it in ether (25mL) to prepare a solution. Under the protection of nitrogen, first add methyl bromide in ether solution (6mL) to the above reaction solution. Add the remaining ether solution of methyl bromide dropwise, add ether (20mL), raise the temperature to keep boiling slightly, and reflux for half an hour; b. Synthesis of intermediate 1-2: under nitrogen protection, use the prepared methyl Grignard reagent with Cool in ice water, add dropwise a solution of 6-oxaspiro[4.5]decane-8,10-dione (10.0g, 59mmol) in ether (20mL) under stirring, control the rate of addition, keep the reaction solution slightly boiling, dropwise After the end, continue to stir at 25 degrees Celsius for half an hour, and white solids are precipitated in the reaction solution. T...
Embodiment 2
[0030]
[0031] The first step: the operation steps and raw material dosage are the same as the first step reaction of Example 1, and the reaction obtains compound 2-2 (10.5g, 52mmol, 88.2%);
[0032] The second step: the operation steps are the same as the second step reaction of Example 1, wherein reactants and charging amount: intermediate 1-2 (10.3g, 51mmol) is replaced by intermediate 2-2 (10.5g, 52mmol), propylene Acyl chloride (9.4g, 104mmol) was replaced by methacryloyl chloride (11g, 105mmol), triethylamine (21.0g, 208mmol) was replaced by triethylamine (21.3g, 210mmol) to obtain compound 2-3 (14.4g, 43mmol, 81.6%).
Embodiment 3
[0034]
[0035] The first step, the operating steps are the same as the first step in Example 1, wherein methyl bromide (11.3g, 119mmol) is changed to ethyl bromide (13g, 119mmol), to obtain compound 3-2 (11.2g, 49mmol, 82.5% );
[0036] The second step: the operation steps are the same as the second step of Example 1, wherein reactant and charging amount: intermediate 1-2 (10.3g, 51mmol) is replaced by 3-2 (11.2g, 49mmol), triethylamine ( 21.0g, 208mmol) was replaced by triethylamine (19.9g, 197mmol), and acryloyl chloride (9.4g, 104mmol) was replaced by acryloyl chloride (8.9g, 98mmol) to obtain compound 3-3 (13.5g, 40mmol, 81.8%) .
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com