HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 733301Erstellt: 25. Oktober 2026
Sulfuric Acid → 2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochloride
https://huagongshe.com/reaction/733301
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | N-Methylol-alpha-chloroacetamide | HCID 62466 | — |
| Edukt | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochloride | HCID 45259771 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07589127B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-23a49715451e4796a490a7c68dc6fa5b |
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| Quellennotiz | uspto-grants-2009_09 |
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