HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381985Generated: October 27, 2026
Diethyl Ether → N-cyanomethyl-2-chloroisonicotinamide
https://huagongshe.com/reaction/1381985
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aminoacetonitrile sulfate (1:1) | HCID 196971 | — |
| Reactant | 2-Chloropyridine-4-carbonyl chloride | HCID 2800003 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-cyanomethyl-2-chloroisonicotinamide | HCID 14054581 | 81.2% |
Reaction Steps
2.4 g (0.056 mol) of sodium hydroxide was dissolved in 24 ml of water. 3.6 g (0.017 mol) of aminoacetonitrile sulfate was added to the solution and the mixture was stirred at room temperature for 1 h and then cooled to 5° C. or below. A liquid mixture of 3.0 g (0.017 mol) of 2-chloroisonicotinoyl chloride and 30 ml of ether was added dropwise thereto at 5° C. or below lest unfavorable heat generation should occur. The mixture was then stirred at room temperature for 2 h to conduct a reaction. Water and ethyl acetate were added thereto to conduct extraction. The extract was washed with a saturated aqueous common salt solution, dried over anhydrous sodium sulfate and concentrated. The resulting crystals were recrystallized from a liquid mixture of n-hexane and ethyl acetate to obtain 2.7 g (yield: 81.2%) of the intended product as white crystals having a melting point of 131° to 132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04804762 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-84880bc6d7f541aeb60720a6915b07e0 |
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| Source note | uspto-grants-1989_02 |
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