HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843876Generated: November 1, 2026
Ethyl Acetate → 2-(Trifluoromethyl)phenylacetonitrile
https://huagongshe.com/reaction/1843876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-(Bromomethyl)-2-(trifluoromethyl)benzene | HCID 123057 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(Trifluoromethyl)phenylacetonitrile | HCID 76435 | 88.5% |
Reaction Steps
A solution of 1-bromomethyl-2-trifluoromethyl-benzene (3.5 g, 14.641 mmol) in DMSO (18 mL) and sodium cyanide (1.076 g, 21.962 mmol) were taken in a flask and the flask was heated to 90° C. for 3 hours. The reaction was monitored by TLC (2% ethylacetate in hexane). The reaction mixture was partitioned between water and ethylacetate. The organic layer was washed with brine solution, dried over Na2SO4 and concentrated to afford 2.4 g of the crude product which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946260B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-083f6a605b644a6ea5d6741bbb90912e |
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| Source note | uspto-grants-2015_02 |
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