HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889531Generated: November 1, 2026
Benzyl Bromide → Benzyl 5-cyano-2-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/889531
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 5-Chloro-2-(trifluoromethyl)benzoic acid | HCID 2773859 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | HCID 178454917 | HCID 178454917 | — |
| Product | Benzyl 5-cyano-2-(trifluoromethyl)benzoate | HCID 67970345 | 57% |
Reaction Steps
Under a nitrogen atmosphere, to a solution of 5-chloro-2-(trifluoromethyl)benzoic acid (5.02 g, 22.35 mmol, 1.0 equiv) in DMA (45 mL), add zinc(II) cyanide (1.77 g, 15.07 mmol, 0.67 equiv), zinc dust (<10 μM, 330 mg, 5.05 mmol, 0.23 equiv), and bis(tri-tert-butylphosphino)palladium (540 mg, 1.06 mmol, 0.05 equiv). Stir the mixture under a nitrogen atmosphere at 95° C. for 9.5 hours. Add cesium carbonate (13.3 g, 40.82 mmol, 1.83 equiv), then benzyl bromide (3.0 mL, 25.15 mmol, 1.13 equiv), and stir under air at room temperature for 3.5 hours. Concentrate under reduced pressure, add water, and extract with EtOAc. Separate the organic phase and wash with saturated aqueous NaCl, dry over MgSO4, filter, and concentrate under reduced pressure. Subject the resulting crude material to flash chromatography on silica gel eluting with a 0-50% EtOAc/hexanes gradient to give the title compound (3.9 g, 57%). MS (m/z) 306 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252831B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-060b2d212a454d7caae7414001d59693 |
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| Source note | uspto-grants-2012_08 |
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