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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDimethylacetamideHCID 31374—
ReactantBenzyl 2-(benzyloxy)-5-bromobenzoateHCID 17750009—
CatalystPotassium ferrocyanide trihydrateHCID 161067—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
ProductBenzyl 2-benzyloxy-5-cyanobenzoateHCID 1897402872%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110570B2
Source datasetuspto-grants-2012_02
ORD IDord-05281bd2597847fd9a7a65b38c57c19f
Source noteuspto-grants-2012_02