関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nitroethane | HCID 6587 | — |
| 反応物 | 3-Carboxybenzaldehyde | HCID 12077 | — |
| 反応物 | Ammonium Acetate | HCID 517165 | — |
| 反応物 | Ethyl acetate hexane | HCID 21226206 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | Amphetamine | HCID 3007 | 161.5% |
反応手順
To a solution of 1.902 q (12.68 mmol) of 3-carboxybenzaldehyde in 10 mL of glacial acetic acid, was added 2.848 mL (2.970 g, 38.04mmol) of nitroethane and 1.080 g (13.95 mmol) of ammonium acetate. The solution was then heated with stirring under nitrogen in a 110° C. oil bath. Then, all of the solid went into solution near 60° C. and the mixture turned a deep yellow color. After 3 hours, thin layer chromatography with 3:1 hexane/EtOAc indicated that no starting material remained. The reaction mixture was cooled to room temperature, and then partitioned between water and methylene chloride, with acidification to about pH2 with 6 M HCl. The organic layer was washed with 6 M HCl, then dried with magnesium sulfate. The solvents were then removed with a rotary evaporator, yielding 2.768 g (98%) of crude material, which was carried on without further purification because of the difficulty of chromatographing the very polar carboxylic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05262333 |
|---|
| 出典データセット | uspto-grants-1993_11 |
|---|
| ORD ID | ord-7a70ff8e997d4bfa9b19dbd164d8ecc5 |
|---|
| 出典メモ | uspto-grants-1993_11 |
|---|