関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Allyl Alcohol | HCID 7858 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | 4-Iodobenzyl alcohol | HCID 29012 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 触媒 | Tetrabutylammonium chloride hydrate | HCID 16212273 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-(4-(Hydroxymethyl)phenyl)propanal | HCID 53425276 | — |
反応手順
10.5 mL (152.8 mmol) allylalcohol, 18.8 g (62.2 mmol) Tetrabutylammonium chloride monohydrate, 12.8 g (152.8 mmol) NaHCO3 and 0.75 g (3.1 mmol) Pd(OAc)2 is added to a solution of 15.0 g (62.2 mmol) 4-iodobenzylalcohol in 100 mL DMF at RT under an N2 atmosphere and the reaction solution is heated to 60° C. for 3 h. The solvent is eliminated i.vac., the residue combined with 250 mL EtOAc and 80 mL water and suction filtered through a fibreglass filter. 80 mL NaCl solution are added to the filtrate, the phases are separated and the organic phase is dried over MgSO4. After the desiccant and solvent have been eliminated the residue is purified by column chromatography on silica gel (gradient: cyc/EtOAc 3:1 after cyc/EtOAc 1:1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07452911B2 |
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| 出典データセット | uspto-grants-2008_11 |
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| ORD ID | ord-c091aec98fb744dc835629a691d3c1bb |
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| 出典メモ | uspto-grants-2008_11 |
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