Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724097Generated: November 1, 2026

Isopropanol → (R)-N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate salt

https://huagongshe.com/reaction/1724097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantSodium IodideHCID 5238—
ReactantMethylamineHCID 6329—
ReactantOxalic acid dihydrateHCID 61373—
Reactant(R)-3-iodo-1-phenyl-1-propanolHCID 14476875—
SolventTetrahydrofuranHCID 8028—
Product(R)-N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate saltHCID 131727265—

Reaction Steps

A solution of (R)-3-iodo-1-phenylpropanol (5.0 g, 19 mmol) and catalytic amount of sodium iodide in tetrahydrofuran (20 mL) and 40% aqueous methylamine (40 mL) was stirred at room temperature for 5 hours. The reaction mixture was evaporated to 15 mL and the pH of the solution was adjusted to pH>12 via the addition of aqueous NaOH solution. The mixture was then twice extracted with toluene and the combined extracts were washed with brine. The toluene layer was evaporated to dryness and the residue dissolved in toluene (25 mL) and isopropanol (25 mL) and oxalic acid dihydrate (1.2 g, 9.5 mmol) was added and the mixture was stirred at room temperature for 2 hours. The resulting suspension was filtered and rinsed with toluene/isopropanol to give 3.0 g of (R)—N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate salt as an off-white solid. The solid (2.9 g) was free based with sodium hydroxide solution and extracted with toluene. The extracts were washed with brine and then evaporated to dryness to give 2.2 g of (R)—N-methyl-3-hydroxy-3-phenylpropylamine as an off-white solid [α]D23=36° (c 1, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485754B2
Source datasetuspto-grants-2009_02
ORD IDord-b6515616323c4f9cb2b2d34ac49876be
Source noteuspto-grants-2009_02