関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (4-(Benzyloxy)phenyl)methanol | HCID 70043 | — |
| 反応物 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 反応物 | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-Benzyloxybenzylamine | HCID 4292845 | 81% |
反応手順
To a solution of 4-benzyloxybenzyl alcohol (3.1 g) in toluene (40 ml) were sequentially added diphenylphosphoryl azide (4.8 g) and 1,8-diazabicyclo[5.4.0]undec-7-ene (2.6 g), and the solution was stirred for 25 hours at room temperature. The solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. Obtained by purifying the residue by silica gel column chromatography (hexane-ethyl acetate system), to a solution of the resulting 1-azidomethyl-4-benzyloxybenzene (3.0 g) in tetrahydrofuran (40 ml) were sequentially added water (3 ml) and triethylphosphine (2.0 ml), and the solution was stirred for 1 hour and 10 minutes at room temperature. The reaction solution was concentrated in vacuo, extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (2.5 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07612114B2 |
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| 出典データセット | uspto-grants-2009_11 |
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| ORD ID | ord-3b87955c2f6a45379aae11a6f8fa50f5 |
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| 出典メモ | uspto-grants-2009_11 |
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