HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443447Generated: October 30, 2026
Potassium thiocyanate → 5-Thiocyanatopyridine-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/443447
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Methyl 5-aminopyridine-2-carboxylate | HCID 12457877 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Thiocyanatopyridine-2-carboxylic acid methyl ester | HCID 12457878 | — |
Reaction Steps
The starting material is prepared as follows: To the solution of 28.3 g of 5-aminopyridine-2-carboxylic acid methyl ester in 80 ml of 20% sulfuric acid, cooled to -4°, the solution of 14.31 g of sodium nitrite in 30 ml of water is added dropwise while stirring and maintaining the temperature below 0°. Thereafter the mixture is stirred for 15 minutes below 0° and the mixture of 28 g of potassium thiocyanate and 8 g of cuprous thiocyanate is added portionwise to said solution. Each addition causes evolution of gas and a black oil to separate. With continued stirring the oil again dissolves and the solution is stirred for 3 hours. It is extracted with methylene chloride, the extract filtered and evaporated, to yield the 5-thiocyanatopyridine-2-carboxylic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04260620 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-e92e4e7174e5467aae9f9da3f17c9fe4 |
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| Source note | uspto-grants-1981_04 |
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