HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558112Generated: November 1, 2026
Trimethylsilyl cyanide → 2-(2-Bromo-4-chlorophenyl)-2-fluoroacetonitrile
https://huagongshe.com/reaction/558112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | 2-Bromo-4-chlorobenzaldehyde | HCID 13154710 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Bromo-4-chlorophenyl)-2-fluoroacetonitrile | HCID 57445060 | 74% |
Reaction Steps
Add 2-bromo-4-chloro-benzaldehyde (3.5 g, 16 mmol) in DCM (6 mL) to a flask that contains zinc iodide (8 mg). Stir the mixture at RT for 30 min. Cool the mixture to 0° C. with an ice-water bath. Add trimethylsilylcyanide (2.14 mL, 15.99 mmol) to the vigorously stirred mixture. Remove the cooling bath and stir at RT for 18 h. Add DCM (20 mL) and cool the mixture to 0° C. Add a solution of diethylaminosulfurtrifluoride (2.32 mL, 18 mmol) in DCM (8 mL) to the previous reaction mixture and stir the mixture overnight. Pour the reaction mixture into ice-water (50 mL) and separate the organic layer. Wash the organic layer with water, 0.5 N HCl, water, saturated NaHCO3, and water. Dry over magnesium sulfate. Remove the organic solvent to give the crude product. Purify by column chromatography (hexane/ethyl acetate, 10:1) to give the title compound (2.40 g, 74%). MS (GC) 249 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063035B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-9c191017a28d4525bf67242fc65128c5 |
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| Source note | uspto-grants-2011_11 |
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