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Hydrogen Bromide → 2-Bromo-5-chloro-2,3-dihydro-1H-inden-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | 5-Chloro-1-indanone | HCID 142599 | — |
| 反応物 | Sodium Bisulfite | HCID 23665763 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-Bromo-5-chloro-2,3-dihydro-1H-inden-1-one | HCID 11334069 | — |
反応手順
A solution of 37.9 g (0.237 mole) of bromine in 120 ml of glacial acetic acid is slowly added dropwise, whilst stirring, to a solution of 40.0 g (0.237 mole) of 5-chloro-1-indanone in 590 ml of glacial acetic acid, to which 0.2 ml of 48% strength aqueous hydrobromic acid has been added. The mixture is stirred for a further 2 hours and the reaction solution is poured into 1 l of water, to which 2.5 g of NaHSO3 have been added. The product, which initially precipitates in the viscous form, becomes crystalline after stirring for a relatively long time. The crude product is filtered off (melting point 69°-76° C.), washed with water and recrystallized from petroleum ether. The pure 2-bromo-5-chloro-1-indanone melts at 89°-90° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04174397 |
| 出典データセット | uspto-grants-1979_11 |
| ORD ID | ord-bda33951a12b4d7bb06da4765a8bf10e |
| 出典メモ | uspto-grants-1979_11 |