HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173295Generated: October 25, 2026
Sulfuric Acid → N-(4-tert-butyl-2-hydroxybenzyl)-2-chloroacetamide
https://huagongshe.com/reaction/1173295
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Phenol, 3-(1,1-dimethylethyl)- | HCID 11450 | — |
| Reactant | N-Methylol-alpha-chloroacetamide | HCID 62466 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-(4-tert-butyl-2-hydroxybenzyl)-2-chloroacetamide | HCID 66746309 | — |
Reaction Steps
A finely powdered mixture of 15 g (0.10 mol) of 3-tert-butylphenol and 12.4 g (0.10 mol) of N-hydroxymethyl-2-chloroacetamide was added in portions to a vigorously stirred solution of 90 mL acetic acid and 10 mL (98%) sulfuric acid at 0° C. The reaction mixture was allowed to warm to room temperature over several hours, and stirring was maintained for a total of 20 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 10-30% 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 | US07834062B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-72a6e4d54eec459abaa7566e8228694e |
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| Source note | uspto-grants-2010_11 |
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