HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzonitrile → HCID 22503375, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzonitrile | HCID 70129 | — |
| Reactant | n-Methyl-2-methylthiophene-3-carboxamide | HCID 22503091 | — |
| Reactant | HCID 178420697 | HCID 178420697 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22503375 | HCID 22503375 | 30% |
Reaction Conditions
| Temperature | -70 °C |
|---|
Reaction Steps
To a solution of N-methyl-2-methylthiophene-3-carboxamide (36.0 g) in THF (500 ml) was added dropwise 2.5M n-BuLi/THF solution (200 ml) at −70° C. The reaction solution was stirred at −70° C. for 2 hr, followed by the addition of anisonitrile (31.0 g) at once. After the dry ice/acetone bath was removed, the reaction mixture was back to room temperature. Three hours later, an aqueous solution of saturated ammonium chloride and ether were added thereto, and then the mixture was further stirred for 1 hr. The resulting white precipitates were collected by filtration, washed with water, ether and n-hexane in this order, and then dried, to give the title compound (17.9 g, yield; 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790844B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-68edf2d14c8e46e693393f712a601978 |
| Source note | uspto-grants-2004_09 |