HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586093Generated: November 1, 2026
4-tert-Butylphenol → 4-(4-tert-Butylphenoxy)benzaldehyde
https://huagongshe.com/reaction/1586093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-tert-Butylphenoxy)benzaldehyde | HCID 10824840 | 95.2% |
Reaction Steps
A mixture of 4-fluorobenzaldehyde (2.0 g, 0.0161 mol), 4-tert-butylphenol (2.42 g, 0.161 mol), and K2CO3 (9.0 g, 0.065 mol) in DMF (50 mL) was heated at 80° C. After 6 h, the reaction mixture was filtered into ice/water and the product was extracted with ethyl acetate. The organic layer was washed with water, dried (MgSO4), concentrated and chromatographed with 1:1 hexane/ethyl acetate to give 3.9 g (95%) of 4-(4-tert-butylphenoxy)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05942532 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-c3b441a713bf4699b13d7e77dd392feb |
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| Source note | uspto-grants-1999_08 |
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