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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814721Generated: October 28, 2026

Triphenylamine → Benzaldehyde, 4-(diphenylamino)-

https://huagongshe.com/reaction/1814721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylamineHCID 11775—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium Acetate TrihydrateHCID 23665404—
SolventAcetoneHCID 180—
ProductBenzaldehyde, 4-(diphenylamino)-HCID 7784673%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878468B2
Source datasetuspto-grants-2005_04
ORD IDord-2127450570684b90b793a3eb38c01bd1
Source noteuspto-grants-2005_04