HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904054Generated: November 2, 2026
Hydrochloric Acid → 2,4-tert-butyl-6-hydroxym ethyl-phenol
https://huagongshe.com/reaction/1904054
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2,4-Di-tert-butylphenol | HCID 7311 | — |
| Reactant | Boric Acid | HCID 7628 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 2,4-tert-butyl-6-hydroxym ethyl-phenol | HCID 526203 | — |
Reaction Steps
2,4-Di-t-butylphenol (20.63 gr., 0.1 mole), paraformaldehyde (3.0 gr., 0.1 mol), boric acid (6.18 g., 0.1 mol) and toluene (50 ml.) were charged into a flask and heated at 80° C. under nitrogen for 48 hours. The mixture was filtered and the solvent removed to provide a brown oil. This oil was dissolved in ether and stirred with an equal volume of 1 N HCl for 2 hours. The ether layer was removed, washed with water, dried (MgSO4) and evaporated to form a soft yellow solid. This solid was stirred in pentane and then filtered to afford a white solid with a melting point of 97°-99° C. The structure was confirmed by NMR and FD/MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04439564 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-d3c16c24d6894ae9be01a77253f270db |
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| Source note | uspto-grants-1984_03 |
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