HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639535Generated: November 2, 2026
Sodium Carbonate → Benzyl 2-benzyloxy-5-cyanobenzoate
https://huagongshe.com/reaction/1639535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Benzyl 2-(benzyloxy)-5-bromobenzoate | HCID 17750009 | — |
| Catalyst | Potassium ferrocyanide trihydrate | HCID 161067 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 2-benzyloxy-5-cyanobenzoate | HCID 18974028 | 72% |
Reaction Steps
A mixture of 695 mg (1.76 mmol) of benzyl 2-benzyloxy-5-bromobenzoate, 175 mg (0.41 mmol) of potassium hexacyanoferrate(II) trihydrate, 41 mg (0.8 mmol) of palladium(II) acetate, and 189 mg (1.75 mmol) of sodium carbonate in 3 mL of dimethylacetamide is heated at 120° C. for 24 hrs. The reaction mixture is diluted with water and extracted several times with ethyl acetate. Combined extracts are washed with brine and dried over Na2SO4. After solvent removal by rotoevaporation, the crude product is purified by preparative TLC to give 436 mg (1.27 mmol, 72% yield) of benzyl 2-benzyloxy-5-cyanobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08110570B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
|---|
| ORD ID | ord-05281bd2597847fd9a7a65b38c57c19f |
|---|
| Source note | uspto-grants-2012_02 |
|---|