HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800561Generated: October 27, 2026
Potassium Carbonate → Methyl 3-(cyanomethoxy)benzoate
https://huagongshe.com/reaction/1800561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Methyl 3-Hydroxybenzoate | HCID 88068 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 3-(cyanomethoxy)benzoate | HCID 14917017 | 86.3% |
Reaction Steps
To a solution of methyl 3-hydroxybenzoate (5.00 g, 32.9 mmol) in acetone (60 mL) were added bromoacetonitrile (2.63 mL, 39.4 mmol) and potassium carbonate (6.81 g, 49.3 mmol), and the mixture was stirred at 60° C. for 4 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution (100 mL), and the mixture was extracted with ethyl acetate (100 mL, 30 mL). The combined organic layer was washed with saturated brine (10 mL), and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=90/10→80/20), and fractions containing the object product were concentrated under reduced pressure to give the title compound (5.43 g, 86%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08344135B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-254488ea0e6647c8bfcaa00f73c59c3d |
|---|
| Source note | uspto-grants-2013_01 |
|---|