関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromide ion | HCID 259 | — |
| 反応物 | 2-(1,3-Dioxolan-2-yl)-1-benzylpyridinium bromide | HCID 19047490 | — |
| 溶媒 | Hydrogen Bromide | HCID 260 | — |
| 生成物 | Benzo(b)quinolizinium, bromide (1:1) | HCID 202130 | 87.6% |
反応手順
A mixture of 1526.8 g (4.74 mol) of 2-(1,3-dioxolan-2-yl)-1-benzylpyridinium bromide in 9 L of 48% HBr solution was heated on a steam-bath until the bromide dissolved. The mixture was heated (heating mantle) in vacuo (aspirator) to remove HBr solution. The dry residue was suspended in 800 mL of HBr solution, cooled, and 4 L of THF was slowly added. The reaction mixture was filtered to afford 1080 g (87%) of benzo[b]quinolizinium bromide as a green solid. Benzo[b]quinolizinium bromide (586 g) was dissolved in 2.4 L of hot water and filtered to remove an insoluble dark material. The filtrate was cooled in ice-water for 4 h, filtered, and the residue was washed with water, dried in vacuo at room temperature for 9 days to afford 508.8 g (86.8%) of benzo[b]quinolizinium bromide (Formula II: R1 =R2 =R7 =H ;X- =Br-).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05631264 |
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| 出典データセット | uspto-grants-1997_05 |
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| ORD ID | ord-a5a8ecac9ca04ca2aba2803b56f66f74 |
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| 出典メモ | uspto-grants-1997_05 |
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