HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717748Generated: October 31, 2026
Dimethyl Sulfoxide → 2-(6-Methylpyridin-3-yl)acetonitrile
https://huagongshe.com/reaction/717748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 5-(Chloromethyl)-2-methylpyridine | HCID 12214338 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(6-Methylpyridin-3-yl)acetonitrile | HCID 11457715 | — |
Reaction Steps
Sodium cyanide (38.6 g, 787.7 mmol, 1.5 equiv), 5-(chloromethyl)-2-methylpyridine (74.37 g, 527.4 mmol, 1 equiv) and DMSO (750 mL, 10 vol) were charged into a reactor and placed under nitrogen. This exothermic mixture self-heated to ca. 45° C. and was heated to 60° C. After 15 min, TLC (eluent: EtOAc:heptanes 50/50) indicated that the reaction was completed. The mixture was cooled to RT and water (1500 mL, 20 vol) was added slowly; the exotherm was controlled by the addition rate. The solution was extracted with EtOAc (4×750 mL), and the combined organic layer was concentrated under reduced pressure. The resulting oil was purified by chromatography (eluent: EtOAc), to obtain 2-(6-methylpyridin-3-yl)acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193728B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-8f0b3566e9524c7a89f383d111a9c654 |
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| Source note | uspto-grants-2015_11 |
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