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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186891Generated: October 26, 2026

Phenol → (R)-2-methyl-1-(3-phenoxy-propyl)-pyrrolidine

https://huagongshe.com/reaction/1186891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantSodium IodideHCID 5238—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant(2R)-(-)-2-Methylpyrrolidine hydrochlorideHCID 11147704—
SolventAcetonitrileHCID 6342—
Product(R)-2-methyl-1-(3-phenoxy-propyl)-pyrrolidineHCID 6700968277.5%

Reaction Steps

To a round-bottom flask was added phenol (5.0 g, 53.1 mmol), 1-bromo-3-chloropropane (5.52 mL, 55.8 mmol), potassium carbonate (22.0 g, 159 mmol), and acetonitrile (100 mL). The reaction mixture was heated to reflux for 15 h. To this reaction was then added (R)-2-methyl-pyrrolidine hydrochloride (12.9 g, 106 mmol) and sodium iodide (7.96 g, 53.1 mmol) at room temperature. The reaction was continued to reflux for 24 h. After cooled to room temperature, the reaction was filtered through a pad of Celite eluted with CH2Cl2 (100 mL). The filtrate was concentrated. Purification by column chromatography (5% MeOH in CH2Cl2) to give 9.02 g (77%) of (R)-2-methyl-1-(3-phenoxy-propyl)-pyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673916B2
Source datasetuspto-grants-2014_03
ORD IDord-86c2c7326e7e4e6fb72631171b57d556
Source noteuspto-grants-2014_03