関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | N-Methylol-alpha-chloroacetamide | HCID 62466 | — |
| 反応物 | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochloride | HCID 45259771 | — |
反応手順
A finely powdered mixture of 5.2 g (25 mmol) of 3,5-di-tert-butylphenol and 3.15 g (25 mmol) of N-hydroxymethyl-2-chloroacetamide was added in portions to a vigorously stirred solution of 22.5 mL acetic acid and 2.5 mL (98%) sulfuric acid at 0-10° C. The reaction mixture was allowed to warm to room temperature over several hours, and stirring was maintained for a total of 16 hours. The reaction mixture was poured into ice-water, neutralized with saturated aqueous NaHCO3 solution and extracted into CH2Cl2. The organic extracts were combined, washed with brine, dried (Na2SO4), filtered and evaporated. The residue was purified on a silica gel flash chromatography column eluted with 15-30-50% EtOAc in hexane. Evaporation of the purified fractions and drying in vacuo afforded the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07589127B2 |
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| 出典データセット | uspto-grants-2009_09 |
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| ORD ID | ord-23a49715451e4796a490a7c68dc6fa5b |
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| 出典メモ | uspto-grants-2009_09 |
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