HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576664Generated: November 1, 2026
4-Hydroxybenzaldehyde → 4-((2',6'-Dimethyl-[1,1'-biphenyl]-3-yl)methoxy)benzaldehyde
https://huagongshe.com/reaction/576664
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3-(2,6-Dimethylphenyl)benzyl alcohol | HCID 23082720 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-((2',6'-Dimethyl-[1,1'-biphenyl]-3-yl)methoxy)benzaldehyde | HCID 86691512 | 80.5% |
Reaction Steps
To a solution of (2′,6′-dimethyl-[1,1′-biphenyl]-3-yl)methanol (1.0 g), 4-hydroxybenzaldehyde (0.58 g), and triphenylphosphine (1.48 g) in tetrahydrofuran (10 mL), a solution of 40% diisopropylazodicarboxylic acid diisopropyl in toluene (1.09 mL) was added under ice-cooling and the resultant reaction mixture was stirred under ice-cooling for 3 hours. A solution of diisopropyl azodicarboxylate in toluene (0.6 mL) was further added and the resultant reaction mixture was stirred at room temperature for 12 hours. From the reaction mixture, the solvent was removed by evaporation under reduced pressure to give a residue and water was added to the resultant residue. The mixture was extracted with an organic solvent and the resultant organic phase was dried over anhydrous sodium sulfate. From the organic phase, the solvent was removed by evaporation under reduced pressure and the resultant residue was purified by silica gel column chromatography (eluent; n-heptane:ethyl acetate=100:0 to 100:20) to give the title compound (1.2 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040525B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-e0b36f4904cd467585a969a910512f46 |
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| Source note | uspto-grants-2015_05 |
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