Micro-Reaction System for Continuous 2-Methyl-4-Amino-5-Aminomethyl Pyrimidine Synthesis

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Solution Overview

Problem

Current methods for preparing 2-methyl-4-amino-5-aminomethyl pyrimidine are inefficient, energy-intensive, and not suitable for industrial production due to long synthetic routes, high costs, and environmental pollution, with traditional batch reactors failing to achieve continuous preparation.

Innovation Solution

A micro-reaction system comprising a micro-mixer and a micro-channel reactor, where a modified Raney nickel catalyst is used for catalytic hydrogenation of 2-methyl-4-cyanopyrimidine, enabling continuous synthesis with improved automation, efficiency, and safety.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If traditional batch reactors are used for preparing 2-methyl-4-amino-5-aminomethyl pyrimidine, then the synthesis can be performed with existing equipment, but the reaction time is long, energy consumption is high, and continuous preparation cannot be achieved

Engineering Contradiction:
Improvereaction timeVSAvoidreaction system complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The traditional batch reactor is segmented into a micro-mixer and a micro-channel reactor. The micro-mixer separates the mixing function while the micro-channel reactor performs the reaction, allowing continuous operation and significantly reducing reaction time from hours to minutes.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The reaction system transitions from a macro-scale batch reactor to a micro-scale continuous flow system. This dimensional change enables continuous preparation, improves heat and mass transfer efficiency, and reduces reaction time while maintaining controllability.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

2Reliability

If catalytic hydrogenation is performed in traditional batch reactors, then the process can be simplified, but high reaction pressure and safety risks remain

Engineering Contradiction:
ImprovesafetyVSAvoidreaction pressure
Core Design Contradiction:
ReliabilityVSStress or pressure

Solution Approach 1:

The micro-channel reactor uses thin-walled structures with precise pressure control, allowing high-pressure hydrogenation reactions to be conducted safely. The small channel dimensions and controlled pressure distribution reduce safety risks while maintaining reaction efficiency.

Inventive Principle:
Principle #30Flexible shells and thin films

Solution Approach 2:

The reaction pressure is optimized for continuous flow conditions in the micro-channel reactor, achieving effective hydrogenation at lower pressures compared to traditional batch reactors. This parameter optimization reduces safety risks while maintaining product yield.

Inventive Principle:
Principle #35Parameter changes

3Extent of automation

If traditional batch processing is used, then equipment requirements are simple, but automation degree and production efficiency are low

Engineering Contradiction:
Improveautomation degreeVSAvoidproduction efficiency
Core Design Contradiction:
Extent of automationVSProductivity

Solution Approach 1:

The system implements continuous flow processing where substrates are continuously fed through the micro-mixer and micro-channel reactor, eliminating idle time between batches. This continuous operation significantly improves production efficiency and enables higher automation.

Inventive Principle:
Principle #20Continuity of useful action

Solution Approach 2:

The micro-reaction system is designed for automated operation with continuous feeding and product collection, reducing manual intervention. The system self-regulates the reaction process through controlled flow rates and integrated separation, improving both automation and efficiency.

Inventive Principle:
Principle #25Self-service

4Ease of manufacture

If conventional synthesis methods are used, then the process is well-established, but the synthetic route is long and cost is high

Engineering Contradiction:
Improvesynthesis route simplicityVSAvoidsynthetic time
Core Design Contradiction:
Ease of manufactureVSLoss of time

Solution Approach 1:

The substrate 2-methyl-4-amino-5-cyanopyrimidine is pre-prepared and purified before being fed into the continuous flow hydrogenation system. This preliminary preparation allows the subsequent reaction to proceed directly and continuously, shortening the overall synthetic route and time.

Inventive Principle:
Principle #10Preliminary action

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The method significantly reduces reaction time, energy consumption, and production costs, achieving high yields (>99%) with a continuous, intrinsically safe process, suitable for industrial production.

Implementation Method 1

modifying a Raney nickel catalyst with formalin to obtain a modified Raney nickel catalyst; allowing the reaction mixture flowing out of the micro-mixer to enter into the micro-channel reactor; and subjecting the reaction mixture to catalytic hydrogenation

Methodology Applied
Scientific EffectCatalysis: Catalysis

Data Source

PatentUS11554354B2Micro-reaction system and method for preparing 2-methyl-4-amino-5-aminomethyl pyrimidine
Publication Date: 2023.01.17 FUDAN UNIVERSITY
  • US11554354B2 patent drawing
  • US11554354B2 patent drawing
  • US11554354B2 patent drawing

AI summary

A micro-reaction system and a method for preparing 2-methyl-4-amino-5-aminomethyl pyrimidine. A Raney nickel catalyst is modified with formalin, and the modified Raney nickel catalyst is filled into a micro-channel reactor of the micro-reaction system. A substrate solution containing 2-methyl-4-amino-5-cyanopyrimidine and a base and hydrogen are transported to the micro-mixer and the micro-channel reactor in sequence for continuous catalytic hydrogenation to obtain 2-methyl-4-amino-5-aminomethyl pyrimidine.