Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 60134565 | HCID 60134565 | — |
| Product | HCID 67310066 | HCID 67310066 | 85% |
Reaction Steps
tert-Butyl 2-methyl-1-morpholinopropan-2-ylcarbamate (640 mg, 2.5 mmol) was dissolved in methyl iodide (20 ml) and placed in a sealed tube. The reaction was stirred at 50° C. for 18 hours. The reaction mixture was concentrated and partitioned between water and ethyl acetate. The water layer was separated and concentrated to give 840 mg (85%) 4-(2-(tert-butoxycarbonylamino)-2-methylpropyl)-4-methylmorpholin-4-ium iodide. 1H NMR (D2O): δ (m, 4 H), 3.83 (s, 2 H), 3.72-3.54 (m, 4 H), 3.37 (s, 3 H), 1.50 (s, 6 H), 1.45 (s, 9 H); MS (ESI+) calculated for C14H29N2O3+: 273.22, Found: 273 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278482B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-2375e7108c55492ebe6be28d4d4bb3bc |
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| Source note | uspto-grants-2012_10 |
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