HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Methyl 5-cyano-2-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | Methyl 2-methoxy-5-formylbenzoate oxime | HCID 86583897 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-cyano-2-methoxybenzoate | HCID 18464789 | — |
Reaction Steps
Combine methyl 2-methoxy-5-formylbenzoate oxime (3.5 g, 16.7 mmol) in dichloromethane (75 mL) and cool in an ice-bath. Add dropwise thionyl chloride (2.0 mL, 27.2 mmol). After 20 minutes, dilute the reaction mixture with dichloromethane and extract with a saturated aqueous solution of sodium bicarbonate and then brine. Dry the organic layer over MgSO4, filter, and concentrate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 1/1 ethyl acetate/hexane to give methyl 2-methoxy-5-cyanobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861417 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-9e709eaa0bab4f4f9b48bd7ef127e42b |
| Source note | uspto-grants-1999_01 |