Preparation method of 2-chloromethyl-3,4-dimethoxypyridine hydrochloride
A technology of dimethoxypyridine hydrochloride and picoline, applied in the field of 2-chloromethyl-3, can solve the problems of low yield, increased cost, low purity and the like
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0015] (1) Add 31.5g of maltol to 20g of sodium hydroxide aqueous solution, stir, cool to 0°C in an ice water bath, slowly add 63 dimethyl phosphate dropwise, control the temperature at 2°C, continue in the ice water bath after dropping After stirring for 3h, pour the mixed solution into 5% 100ml sodium hydroxide solution, stir, extract three times with dichloromethane, wash the extract with water until it is neutral, add anhydrous sodium sulfate to dry, heat in a water bath to evaporate the solvent, Distill under reduced pressure to obtain 19.8 g of colorless liquid 3-methoxy-2-methyl-4H-pyran-4-one with a yield of 77%;
[0016] (2). Add 13.2g of 3-methoxy-2-methyl-4H-pyran-4-one to 360mld of concentrated ammonia water, stir at 40°C for 3h, evaporate the water under reduced pressure, the residue Cool, precipitate crystals, filter, wash the filter cake with water to neutrality, and recrystallize it with acetone to obtain 10.1 g of white crystals of 3-methoxy-2-methyl-4(1H)-pyrido...
Embodiment 2
[0023] (1) Add 50g of maltol to 25g of sodium hydroxide aqueous solution, stir, cool to 2°C in an ice water bath, slowly add 80g of dimethyl phosphate dropwise, control the temperature at 4°C, continue to stir in the ice water bath after dropping 6h, pour the mixed solution into 5% 100ml sodium hydroxide solution, stir, extract with dichloromethane three times, wash the extract with water until it is neutral, add anhydrous sodium sulfate to dry, heat in a water bath to evaporate the solvent, and then reduce 38.6g of colorless liquid 3-methoxy-2-methyl-4H-pyran-4-one was obtained by pressure distillation; the yield was 78%;
[0024] (2). Add 13.2g of 3-methoxy-2-methyl-4H-pyran-4-one to 360ml of concentrated ammonia water, stir at 45℃ for 6h, evaporate the water under reduced pressure, and cool the residue to separate out After the crystals were filtered, the filter cake was washed with water to neutrality, and then recrystallized with acetone to obtain 11.1 g of white crystals of...
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