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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627955Generated: November 2, 2026

3-Phenylprop-2-En-1-Ol → N-Methyl-N-(3-phenylprop-2-en-1-yl)aniline

https://huagongshe.com/reaction/1627955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenylprop-2-En-1-OlHCID 308—
ReactantN-MethylanilineHCID 7515—
ReactantMethyl formateHCID 7865—
ReactantPotassium CarbonateHCID 11430—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventSodium chloride; waterHCID 57417360—
ProductN-Methyl-N-(3-phenylprop-2-en-1-yl)anilineHCID 5382506292%

Reaction Steps

Cinnamyl alcohol (100 mg, 0.75 mmol), N-methylaniline (53 mg, 0.50 mmol), dppf (14 mg, 0.025 mmol), K2CO3 (207 mg, 1.5 mmol) and [Pd(allyl)Cl]2 (4.5 mg, 0.0125 mmol) were sequentially added under argon to a reaction tube equipped with a stir bar and a septum. Degassed TPGS-M-PEG-750 solution (1.0 mL, 2 wt %), and HCO2Me (0.12 mL, 2.0 mmol) were added by syringe and vigorously stirred for 20 h. After the reaction, the contents of the flask were diluted with brine and extracted with EtOAc. The solution obtained was dried over anhydrous MgSO4, filtered, and concentrated by rotary evaporation. The residue was purified by flash chromatography eluting with 10% EtOAc/hexanes to afford the product as a pale yellow liquid (102 mg, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785665B2
Source datasetuspto-grants-2014_07
ORD IDord-002d83de58fa4af3832c5e34cfdce71e
Source noteuspto-grants-2014_07