Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86597964 | HCID 86597964 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11240761 | HCID 11240761 | 85.6% |
Reaction Steps
(3R,4R,5R)-3-Amino-4,5-dimethyl-heptanoic acid hydrochloride (10.8 g, 51.5 mmol) was dissolved in 50 mL of methanol. To this solution was added triethylamine (5.2 g, 7.2 mL, 51.5 mmol). The solution was stirred for 10 minutes and then evaporated to a flocculent solid. Dichloromethane (376 mL) was added and the resulting slurry was stirred at room temperature for 45 minutes. Next, 188 mL of acetonitrile was added and the slurry was stirred for 30 minutes and then filtered. The solids were washed with 20 mL of 2:1 (v/v) dichloromethane-acetonitrile and dried on a nitrogen press to give 7.64 g (85.6% yield) of the titled compound as a white solid: 1H NMR (CD3OD, 399.77 MHz) 0.88 (t, J=7.5 Hz, 3H), 0.91 (d, J=7.0 Hz, 3H), 0.94 (d, J=6.6 Hz, 3H), 0.98–1.12 (m, 1H), 1.32–1.43 (m, 1H), 1.43–1.64 (m, 2H), 2.26 (dd, J=16.5, 9.9 Hz, 1H), 2.47 (dd, J=19.5, 3.7 Hz, 1H), 3.28–3.36 (m, 1H). Low resolution mass spec: nominal m/e calc'd for C9H19NO2 (M+H)+: 174. Found: m/e 174.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179934B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-ce3cfde5a12a4f248bcf4e750ad018bb |
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| Source note | uspto-grants-2007_02 |
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