HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 20085211, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 20085198 | HCID 20085198 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20085211 | HCID 20085211 | 61% |
Reaction Steps
To a clear solution of 3-butyl-3-[(1,2,4-triazol-1-yl)methyl]-2(3H)-benzofuranone (5.0 g, 0.0184 mole) and dimethyl formamide (20 mL) in a 300 mL round bottom flask, potassium t-butoxide (6.2 g, 0.0553 mole) was added and the reaction mixture stirred at room temperature for 5 minutes before adding methyl iodide (3.2 g, 0.0221 m). The reaction mixture was stirred with heating at 40° C. for 1 hour and 1.0 g of water was added. The stirring was continued for an additional 2 hours at 40° C., before adding 100 mL of water and 100 mL of ethyl ether for work up. The organic phase was isolated and dried over magnesium sulfate, evaporated by rotary evaporator to afford 4.0 g of oily concentrate (yield 61%), Example 69 of Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05397768 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-72687c0e3b8d4041a65f99fad6879d9e |
| Source note | uspto-grants-1995_03 |