関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Monobenzone | HCID 7638 | — |
| 反応物 | Cyanomethylenetributylphosphorane | HCID 4622928 | — |
| 反応物 | Methyl 2-((4-(3-hydroxypropyl)phenoxy)methyl)benzoate | HCID 10780567 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoate | HCID 68869717 | 64.3% |
反応手順
Methyl 2-{[4-(3-hydroxypropyl)phenoxy]methyl}benzoate (0.50 g, 1.66 mmol) and 4-(benzyloxy)phenol (0.33 g, 1.66 mmol) was added to a dry round bottomed flask fitted with a septum Dry toluene (10 ml) was added and N2 was flushed through the mixture for 5 minutes. (Tributylphosphoranylidene)acetonitrile (0.80 g, 3.33 mmol) was added dropwise and the reaction was performed in a single node microwave oven. After removing the solvent by evaporation the crude was purified by preparative HPLC (started with acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min)). The product containing fractions were pooled and the acetonitrile was removed by evaporation. EtOAc (10 ml) was added and the organic phase was washed with two portions of brine and dried (MgSO4). Removing the solvent by evaporation gave 0.515 gram of methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]-propyl}phenoxy)methyl]benzoate (yield 64.1%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07521461B2 |
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| 出典データセット | uspto-grants-2009_04 |
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| ORD ID | ord-368ce849ae60442aba721e0c86c78c50 |
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| 出典メモ | uspto-grants-2009_04 |
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