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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628374Generated: November 1, 2026

Benzaldehyde, 4-(diphenylamino)- → Benzenamine, 4-ethenyl-N,N-diphenyl-

https://huagongshe.com/reaction/1628374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehyde, 4-(diphenylamino)-HCID 77846—
ReactantHCID 22020909HCID 22020909—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductBenzenamine, 4-ethenyl-N,N-diphenyl-HCID 10869403—

Reaction Steps

19 g of methylphosphonium bromide is suspended in dried THF under protective gas, and 6 g of potassium tert-butoxide are added in portions at 0° C. An immediate colour change to orange occurs. 14 g of N,N-diphenyl-p-aminobenzaldehyde are added to the reaction solution at 0° C. The mixture is warmed to room temperature and stirred for a further 20 hours. The solvent is stripped off in vacuo, the residue is taken up in dichloromethane, and the solution is extracted with water dried over magnesium sulfate, filtered, and the solvent is stripped off in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08786181B2
Source datasetuspto-grants-2014_07
ORD IDord-9f6f2090a097422382edb0eb7c12b0cf
Source noteuspto-grants-2014_07