HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436260Generated: October 30, 2026
Phenylacetonitrile → HCID 20520018, compound
https://huagongshe.com/reaction/436260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,6-Dichloro-3-nitropyridine | HCID 85239 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20520018 | HCID 20520018 | — |
Reaction Steps
There were gradually added to a cooled and stirred solution of 190 grams of 2,6-dichloro-3-nitropyridine and 117 grams of benzyl cyanide in 2 liters of dioxane under a nitrogen atmosphere 64 grams of sodium hydride (80% in white oil). The reaction mixture immediately turned a deep dark blue color, gradually a finely divided precipitate began to separate out, the temperature rose (with cooling with ice water) to 30° C. After 3 hours the mixture was treated with about 20 ml of ethyl alcohol, stirred for another 20 minutes, then filtered with suction. The deep blue sodium salt was dissolved in 1 liter of water, treated with dilute acetic acid until the color changed. The 2-(α-cyanobenzyl)-3-nitro-6-chloropyridine formed crystallized out in pure form. M.P. 165° C; Yield 146 grams.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04008223 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-bdb3fde70ab64ca1ab0406495338c9e6 |
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| Source note | uspto-grants-1977_02 |
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