HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100683Generated: October 31, 2026
Sodium Chloride → [3-Chloro-5-(trifluoromethyl)pyridin-2-yl]acetonitrile
https://huagongshe.com/reaction/2100683
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 49757460 | HCID 49757460 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | [3-Chloro-5-(trifluoromethyl)pyridin-2-yl]acetonitrile | HCID 16227272 | — |
Reaction Steps
314 g (1.13 mol, 1 eq.) of methyl [3-chloro-5-(trifluoromethyl)-2-pyridinyl]-(cyano)acetate and 22 g (0.38 mol, 0.33 eq.) of sodium chloride are dissolved in a solution of 44 mL of water and 1.1 L of dimethyl sulphoxide. The reaction medium is stirred and heated at 160° C. Once all gas has been given off, the medium is cooled to ambient temperature. 1 L of water and 0.5 L of dichloromethane are added. After separation, the aqueous phase is extracted twice with 0.5 L of dichloromethane. The organic phase is washed twice with 0.5 L of water and dried over magnesium sulphate. After concentration, the crude product is diluted in 100 mL of dichloromethane and eluted with an ethyl acetate/heptane mixture (20/80) on a bed of silica. The filtrate is concentrated so as to produce [3-chloro-5-(trifluoromethyl)-2-pyridinyl]acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572818B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-bb2033ece0894bc79ffa8328645415da |
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| Source note | uspto-grants-2009_08 |
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