戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 733301作成日:2026年10月27日

Sulfuric Acid → 2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochloride

https://huagongshe.com/reaction/733301

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物N-Methylol-alpha-chloroacetamideHCID 62466—
反応物3,5-Di-tert-butylphenolHCID 70825—
反応物Sodium BicarbonateHCID 516892—
溶媒Acetic AcidHCID 176—
生成物2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07589127B2
出典データセットuspto-grants-2009_09
ORD IDord-23a49715451e4796a490a7c68dc6fa5b
出典メモuspto-grants-2009_09