Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724096Generated: November 2, 2026

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

https://huagongshe.com/reaction/1724096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantSodium IodideHCID 5238—
ReactantMethylamineHCID 6329—
ReactantOxalic acid dihydrateHCID 61373—
Reactant(1R)-3-chloro-1-phenylpropan-1-olHCID 642409—
SolventEthanolHCID 702—
Product(R)-N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate saltHCID 131727265—

Reaction Steps

A solution of (R)-3-chloro-1-phenylpropanol (1.0 g, 5.85 mmol) and a catalytic amount of sodium iodide in ethanol (7 mL) and 40% methylamine aqueous solution (15 mL) was stirred at 60° C. for 7 hours. The reaction mixture was evaporated to 3 mL, and the pH of the solution was adjusted to pH>12 via the addition of aqueous NaOH solution. The mixture was then extracted with toluene twice and the combined extracts were washed with brine. The toluene layer was evaporated to dryness and the residue dissolved in toluene (5 mL) and isopropanol (5.mL) and oxalic acid dihydrate (0.4 g, 3.2 mmol) was added. It was stirred at room temperature for 2Hours and the suspension was filtered and rinsed with toluene/isopropanol to provide 0.9 g of (R)—N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate salt as an off-white solid. 1H NMR (D2O) δ 7.5-7.2 (m, 5H), 4.8 (at, J=6.6 Hz, 1H), 5.15-2.9 (m, 2H), 2.64 (s, 3H), 2.2-2.0 (m, 2H). Elemental Analysis for C11H16NO3; Calculated: H 7.67%; C 62.84%; N 6.66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485754B2
Source datasetuspto-grants-2009_02
ORD IDord-464db26ddc9c4dae81070de3b4881d17
Source noteuspto-grants-2009_02