HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733301Generated: October 25, 2026
Sulfuric Acid → 2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochloride
https://huagongshe.com/reaction/733301
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | N-Methylol-alpha-chloroacetamide | HCID 62466 | — |
| Reactant | 3,5-Di-tert-butylphenol | HCID 70825 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochloride | HCID 45259771 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589127B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-23a49715451e4796a490a7c68dc6fa5b |
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| Source note | uspto-grants-2009_09 |
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