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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Oxalic acid dihydrate | HCID 61373 | — |
| Reactant | (1R)-3-chloro-1-phenylpropan-1-ol | HCID 642409 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-N-methyl-3-hydroxy-3-phenylpropylamine hemioxalate salt | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07485754B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-464db26ddc9c4dae81070de3b4881d17 |
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| Source note | uspto-grants-2009_02 |
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