HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → methyl 2-methoxy-5-(1H-triazol-1-ylmethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Methylformamide | HCID 31254 | — |
| Reactant | Methyl 5-(chloromethyl)-2-methoxybenzoate | HCID 240622 | — |
| Reactant | HCID 178418936 | HCID 178418936 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | methyl 2-methoxy-5-(1H-triazol-1-ylmethyl)benzoate | HCID 18464866 | — |
Reaction Steps
Combine triazole (0.72 g, 10.4 mmol) and methylformamide (6 mL). Cool in an ice bath and add sodium hydride (0.42 g, 60% i oil, 10.4 mmol). After 30 minutes, warm to ambient temperature. Add a solution of methyl 2-methoxy-5-chloromethylbenzoate (1.85 g, 6.74 mmol) in dimethylformamide (6 mL). Heat to 75° C. After 3 hours, partition the reaction mixture between water and ethyl acetate. Extract the organic layer with water, dry over Na2SO4, filter, and concentrate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 95/5 dichloromethane/methanol containing 0.5% concentrated aqueous ammonia to give methyl 2-methoxy-5-(1H-triazol-1-ylmethyl)benzoate: Rf=0.1 (silica gel, 1/1 hexane/ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211199B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-81b5f91bc6f5441583bcdef6f4fccec9 |
| Source note | uspto-grants-2001_04 |