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N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine → 2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine | HCID 87682 | — |
| 反応物 | 2-butyl-3,5-dihydro-4H-imidazol-4-one | HCID 10909654 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-one | HCID 136375570 | 77.1% |
反応手順
A solution of 5.00 g (35.67 mmol) of 2-butyl-2-imidazolin-5-one and 7.02 g (39.24 mmol) of N,N-dimethylformamide diisopropyl acetal in 25 ml of methylene chloride was stirred at room temperature for 2.5 hours. Then, the solvent was removed on a Rotavapor, and the residue was treated with 40 ml of methylene chloride. The solution thus obtained was washed twice, each time with 10 ml of water, and dried (MgSO4) and concentrated on the Rotavapor. The residue was then dried in a high vacuum. 5.37 g of 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one was obtained; the product had a content of greater than 90 percent, according to H-NMR. This corresponds to a yield of about 71 percent, based on the 2-butyl-2-imidazolin-5-one.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05486617 |
| 出典データセット | uspto-grants-1996_01 |
| ORD ID | ord-123c54209c5948949a04dc3581b0b0a2 |
| 出典メモ | uspto-grants-1996_01 |