HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249637Generated: November 2, 2026
Formaldehyde → 2,6-Di-tert-butyl-4-methylphenol
https://huagongshe.com/reaction/1249637
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | 91.8% |
Reaction Steps
A 2.5 liter shaker reactor was charged with 2,6-di-t-butylphenol (52 g, 0.25 m), formaldehyde (21 g of 37% aq. solution, 0.25 m), triethylamine (30 g, 0.3 m) and methyl alcohol (200 ml). The mixture was heated at 127° C. for 2 hrs. under a nitrogen blanket with agitation. The mixture was hydrogenated at 160° C. in the presence of nickel catalyst (5 g) and 300 psig of H2. Absorption of hydrogen ceased after 15 minutes. The product, after filtering to remove the catalyst, was distilled to recover methyl alcohol, triethylamine and crude DBPC which was distilled at 128° C./6-8 mm Hg to give 51 g (93 mole % yield) of DBPC. Analysis of DBPC by GC was 97% DBPC and 2.8% 2,6-di-t-butylphenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04633022 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-c8b1848305aa44ecb95a538f2660b0fd |
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| Source note | uspto-grants-1986_12 |
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