HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814721Generated: October 28, 2026
Triphenylamine → Benzaldehyde, 4-(diphenylamino)-
https://huagongshe.com/reaction/1814721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylamine | HCID 11775 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | 73% |
Reaction Steps
30 mL of dimethylformaldehyde (DMF) was put into a 250 mL flask, cooled to 0° C. and 3.8 mL of POCl3 was slowly added thereto. Then, 10 g of triphenylamine was added to the resultant mixture and heated to 70° C. for 5 hours. The reaction container was cooled to room temperature and then a reactant solution was poured into ice water. Subsequently, 40 g of sodium acetate trihydrate was put for neutralization and then an organic layer was separated with methylenechloride. The obtained organic layer was dried using magnesium sulfate and methylenechloride was removed under reduced pressure, yielding a product. The product was recrystallized using methanol and a light yellow solid was finally obtained, yielding 73% of a desired product. Data of NMR spectra confirmed that the product had the same structure as 4-(diphenylamino)benzaldehyde, that is, the compound (1) in the reaction scheme 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878468B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-2127450570684b90b793a3eb38c01bd1 |
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| Source note | uspto-grants-2005_04 |
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