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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795635Generated: November 1, 2026

Benzylamine → N-benzyl-4-methylaniline

https://huagongshe.com/reaction/1795635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant4-ChlorotolueneHCID 7810—
ReactantSodium t-butoxideHCID 23676156—
CatalystBinap, (A+-)-HCID 634876—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductN-benzyl-4-methylanilineHCID 7940390%

Reaction Conditions

Temperature100 °C

Reaction Steps

An oven dried Schlenk tube was purged with argon and charged with Pd2(dba)3 (4.6 mg, 0.005 mmol, 1.0 mol % Pd), Cy-BINAP (9.6 mg, 0.015 mmol, 1.5 mol %), and NaOtBu (135 mg, 1.4 mmol). The tube was purged with argon and charged with toluene (2 mL), 4-chlorotoluene (0.12 mL, 1.0 mmol), and benzylamine (0.165 mL, 1.5 mmol). The mixture was heated to 100° C. with stirring until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was cooled to room temperature, diluted with ether (20 mL), filtered through celite, and concentrated in vacuo. The crude material was then purified by flash chromatography on silica gel to give 177 mg (90%) of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026498B2
Source datasetuspto-grants-2006_04
ORD IDord-050b9c3d5bd54310b747ef05325f2b6d
Source noteuspto-grants-2006_04