The efficient synthesis and thorough understanding of chemical intermediates are cornerstones of progress in chemistry. 1-Ethyl-7-nitro-1,2,3,4-tetrahydroquinoline (CAS 57883-28-0) is a compound of significant interest, offering a foundation for various synthetic endeavors. As a dedicated manufacturer and supplier, our focus is on providing researchers with high-quality materials and detailed information. This article outlines the common synthesis routes and key properties of this valuable intermediate, guiding those who wish to buy it.

Synthetic Methodologies

The preparation of 1-Ethyl-7-nitro-1,2,3,4-tetrahydroquinoline typically involves two main stages: the introduction of the nitro group and the subsequent alkylation of the nitrogen atom. Common approaches include:

  1. Selective Nitration: The parent 1,2,3,4-tetrahydroquinoline can be subjected to nitration conditions, typically using a mixture of nitric acid and sulfuric acid (mixed acid). Careful control of temperature and reaction time is essential to favor substitution at the 7-position, which is electronically favored, while minimizing over-nitration or oxidation. The resulting 7-nitro-1,2,3,4-tetrahydroquinoline is then isolated and purified.
  2. N-Alkylation: The secondary amine nitrogen of the tetrahydroquinoline ring can be alkylated using ethylating agents such as ethyl bromide, ethyl iodide, or diethyl sulfate. This reaction is usually carried out in the presence of a base (e.g., potassium carbonate, triethylamine) in a suitable solvent (e.g., DMF, acetonitrile) to deprotonate the amine and facilitate nucleophilic substitution. Heating may be required to achieve good yields.

Alternatively, a one-pot cascade reaction might be employed for more complex derivatives, but for this specific compound, the sequential approach is common. Our role as a manufacturer involves optimizing these processes to ensure high yields and consistent purity (≥98.0%) for our customers who wish to purchase this intermediate.

Key Physicochemical Properties

  • Appearance: Light Yellow Liquid
  • Molecular Formula: C₁₁H₁₄N₂O₂
  • Molecular Weight: 206.24 g/mol
  • CAS Number: 57883-28-0
  • Purity: ≥98.0%
  • Storage: Stored in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances.

These properties are critical for handling, storage, and application in various chemical processes. As a reliable supplier, we ensure that our product adheres to these specifications, making it easier for researchers to integrate it into their workflows. We offer competitive pricing and can provide quotes for bulk quantities.

Applications in Chemical Research

1-Ethyl-7-nitro-1,2,3,4-tetrahydroquinoline is primarily used as an intermediate in organic synthesis and for the development of pharmaceutical compounds. Its structure allows for diverse functionalization, making it a valuable building block for creating more complex molecules with potential biological activities.

For researchers seeking to buy this compound, partnering with a reputable manufacturer like us ensures access to high-quality material and reliable technical support. We are committed to supporting scientific advancement by providing essential chemical intermediates.