Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 86681543 | HCID 86681543 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71523276 | HCID 71523276 | — |
Reaction Steps
To a solution of 1-(cyclohexyl(methyl)amino)propan-2-yl 2,4,6-trimethylbenzoate (0.30 g, 0.946 mmol) in DCE (5 mL), methyl iodide (0.12 mL, 1.892 mmol) was added. The resultant reaction mixture was stirred at rt for 16 hours. The reaction mixture was diluted with DCM and concentrated to dryness. The crude product was subjected to column chromatography to obtain N,N-dimethyl-N-[2-((2,4,6-trimethylbenzoyl)oxy)propyl]cyclohexanaminium iodide. Yield: 0.109 g (25%). 1H NMR (400 MHz, CDCl3) δ 6.86 (s, 2H), 5.70-5.67 (m, 1H), 4.52-4.48 (d, J=14 Hz, 1H), 3.83-3.77 (m, 1H), 3.70-3.64 (m, 1H), 3.34 (s, 3H), 3.28 (s, 3H), 2.29-2.01 (m, 10H), 2.01-1.98 (m, 1H), 1.84 (m, 1H), 1.64-1.62 (d, J=6 Hz, 4H), 1.47-1.38 (m, 4H), 1.13-1.08 (m, 2H). LCMS: m/z=332.2 [M+], RT=3.01 min (Column: Y, Program: P1). HPLC: 99.53% (200 nm), RT 4.11 min (Mobile phase: A: ACN, B: 0.05% TFA in water, Column: Zorbax® SBC18 (50*4.6 mm) 1.8μ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09180115B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-411133679d404c6bba0f38fd1315869c |
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| Source note | uspto-grants-2015_11 |
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