Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylethylamine | HCID 11723 | — |
| Reactant | Pyrrolidine, 1-(1-cyclopenten-1-yl)- | HCID 81570 | — |
| Reactant | HCID 86644964 | HCID 86644964 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58489078 | HCID 58489078 | 87% |
Reaction Steps
(R)-propyl 2-acetamido-3-chloropropanoate (2.50 g, 12.0 mmol) was dissolved in acetonitrile (25 mL) and 1-pyrrolidino-1-cyclopentene (2.27 mL, 2.14 g, 15.6 mmol) was added. While the reaction was kept at 20° C., dimethylethylamine (1.70 mL, 1.14 g, 15.6 mmol) was added via an addition funnel during 10 min. The homogeneous reaction was stirred at 20° C. for 21 h. Then, water (0.50 mL) was added and the reaction was further stirred for 2.5 h. The solvents were removed in vacuo at 50° C. and the residual oil was purified by silica gel flash chromatography using an EtOAc:petroleum benzene gradient. The product is a yellowish oil. Weight 2.67 g, approx. 87% yield (two diastereomers). 1H NMR: (CDCl3, 300 MHz): δ 6.62 (br d, 0.5H), 6.38 (br d, 0.5H), 4.61-4.49 (m, 1H), 4.05-4.00 (m, 2H), 2.38-1.92 (m, 8H), 1.80-1.47 (m, 6H), 0.90-0.84 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08105807B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e52baaefa349435a8b2cb631d93a389e |
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| Source note | uspto-grants-2012_01 |
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