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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884175Generated: November 1, 2026

Aniline → Diphenylamine

https://huagongshe.com/reaction/1884175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantChlorobenzeneHCID 7964—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductDiphenylamineHCID 1148730.1%

Reaction Steps

The general procedure from Example 1A was followed using chlorobenzene (135 mg, 1.2 mmol) and aniline (93 mg, 1.0 mmol) with Pd2(dba)3 (25 mg, 0.027 mmol) and (Me3C)2PH(O) (7.0 mg, 0.042 mmol) and NaOtBu (144 mg, 1.5 mmol) in 2.0 mL of toluene. After 24 h, the reaction mixture was chromatographed with 5% ethyl acetate/hexane to give 51 mg (30% yield) of diphenylamine. It was >95% pure by 1H NMR and GC/MS. 1H NMR (500 MHz, CDCl3): δ7.18 (m, 4H), 6.99 (d, J=7.68 Hz, 4H), 6.84 (t, J=7.34 Hz, 2H), 5.59 (br, 1H) ppm. 13C NMR (125 MHz, CDCl3): d 143.1, 129.3, 120.9, 117.8 ppm. MS: Calculated for C12H11N(M+): 169.1. Found: 170.3 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762330B2
Source datasetuspto-grants-2004_07
ORD IDord-2533462f77a24145bcac96635368d1d0
Source noteuspto-grants-2004_07