関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-(Chloromethyl)-4-iodobenzene | HCID 817211 | — |
| 反応物 | HCID 86625642 | HCID 86625642 | — |
| 触媒 | Zinc | HCID 23994 | — |
| 触媒 | Bis(1,5-cyclooctadiene)nickel | HCID 6433264 | — |
| 触媒 | 18-(p-Iodophenyl)octadecanol | HCID 11655804 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | HCID 57548711 | HCID 57548711 | 76% |
反応手順
Zinc powder (70 mg, 1.06 mmol) was dried at 70° C. for 30 min in a sealed tube, then DMA (0.4 ml) and solid 12 (9 mg, 0.04 mmol) were added. After stirring for 10 min, a solution of ethyl 17-iodo-heptadecanoate 80 (300 mg, 0.71 mmol) in DMA (1.5 ml) was added and the reaction mixture was stirred in the sealed tube for 11 h at 70° C. In a 10-ml flask, Ni(COD)2 (10 mg, 0.04 mmol), (R)-(s-Bu)-Pybox (or (S)-(s-Bu)-Pybox) (23 mg, 0.07 mmol) and p-iodobenzyl chloride 82 (252 mg, 1 mmol) were dissolved in DMA (1.5 ml), then organozinc solution 81 was added via cannula. The mixture was stirred at room temperature for 15 h, and the reaction was quenched by addition of aqueous NH4Cl, extracted with EtOAc, the extract was dried over Na2SO4 and evaporated. Chromatography of the crude product in hexane-ether (97:3) yielded the compound 37 (276 mg, 76%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07893286B2 |
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| 出典データセット | uspto-grants-2011_02 |
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| ORD ID | ord-c3c51c7e1e64448e9c1e26e6e91eb2b3 |
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| 出典メモ | uspto-grants-2011_02 |
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