![Triethylamine Organic Base Molecule Skeletal Formula Stock Vector (Royalty Free) 1128981863 | Shutterstock Triethylamine Organic Base Molecule Skeletal Formula Stock Vector (Royalty Free) 1128981863 | Shutterstock](https://www.shutterstock.com/image-vector/triethylamine-organic-base-molecule-skeletal-260nw-1128981863.jpg)
Triethylamine Organic Base Molecule Skeletal Formula Stock Vector (Royalty Free) 1128981863 | Shutterstock
Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing)
![Triethylamine organic base molecule. 3D rendering. Atoms are represented as spheres with conventional color coding: hydrogen (white), carbon (grey), n Stock Photo - Alamy Triethylamine organic base molecule. 3D rendering. Atoms are represented as spheres with conventional color coding: hydrogen (white), carbon (grey), n Stock Photo - Alamy](https://c8.alamy.com/comp/R06WT9/triethylamine-organic-base-molecule-3d-rendering-atoms-are-represented-as-spheres-with-conventional-color-coding-hydrogen-white-carbon-grey-n-R06WT9.jpg)
Triethylamine organic base molecule. 3D rendering. Atoms are represented as spheres with conventional color coding: hydrogen (white), carbon (grey), n Stock Photo - Alamy
![Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03125G Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03125G](https://pubs.rsc.org/image/article/2016/NJ/c5nj03125g/c5nj03125g-s2_hi-res.gif)
Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C5NJ03125G
![SOLVED: 3) The intermediate alcohol, depicted in the scheme below; can be converted to its mesylate on treatment with methavesulfonvi chloride and triethylamine: Mesylates are excellent leaving groups which can be displaced SOLVED: 3) The intermediate alcohol, depicted in the scheme below; can be converted to its mesylate on treatment with methavesulfonvi chloride and triethylamine: Mesylates are excellent leaving groups which can be displaced](https://cdn.numerade.com/ask_images/828ad0298b124a84b7e729433fec7be2.jpg)