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2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one → 2-[(2-Chlorophenyl)phenylmethyl]-1-azabicyclo[2.2.2]octan-3-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one | HCID 297405 | — |
| 反応物 | HCID 178418255 | HCID 178418255 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-[(2-Chlorophenyl)phenylmethyl]-1-azabicyclo[2.2.2]octan-3-one | HCID 19797478 | — |
反応手順
2-(2-Chlorobenzylidene)-1-azabicyclo[2.2.2]octan-3-one (3 g) was dissolved in toluene (30 ml) and placed in a dropping funnel. Phenylmagnesium bromide was dissolved in toluene (15 ml) and stirred under nitrogen. This was cooled in an ice/water bath and the benzylidene solution was added dropwise. After 3 hrs the reaction was quenched with ammonium chloride solution and the aqueous layer extracted with dichloromethane (×4); this was combined with the original toluene layer and dried (MgSO4). The solvent was removed in vacuo and the residue purified by chromatography on silica eluting with 1:1 hexane:diethyl ether which afforded the title compound as a 2:1 mixture of its diastereoisomers:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05242930 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-28e88db65242445cb373f341e46ba373 |
| 出典メモ | uspto-grants-1993_09 |