HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184579Generated: October 31, 2026
Potassium tert-butoxide → HCID 86680441, compound
https://huagongshe.com/reaction/1184579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86680440 | HCID 86680440 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86680441 | HCID 86680441 | — |
Reaction Steps
To a solution of 1-tert-butyl 3-methyl 4-(3-methoxy-3-oxopropyl)piperazine-1,3-dicarboxylate (Example 100A, 180 g, 0.545 mol) in tetrahydrofuran (1.3 L) was added potassium t-butoxide (98 g, 0.872 mol) with stirring at 0-5° C. under N2 atmosphere portion-wise over a period of 30 minutes. The reaction mixture was stirred at ambient temperature for 2 hours. The reaction was then quenched with saturated aqueous ammonium chloride solution (500 mL) and extracted with ethyl acetate (1 L). The organic layer was separated, washed with brine (500 mL), dried over Na2SO4, filtered and concentrated to afford the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 1.48 (s, 9H), 2.28-2.35 (m, 2H), 2.65-2.83 (m, 1H), 2.83-3.12 (m, 3H), 3.43 (t, 1H, J=8.4 Hz), 3.61 (t, 1H, J=8.4 Hz), 3.78 (s, 3H), 3.98-4.20 (bs, 1H), 4.20-4.45 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08669255B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-89395c5df5804405981a87d994801d81 |
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| Source note | uspto-grants-2014_03 |
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