HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705689Generated: October 29, 2026
N-Hydroxyacetamidine → HCID 58487604, compound
https://huagongshe.com/reaction/705689
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Hydroxyacetamidine | HCID 30926 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 49761218 | HCID 49761218 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58487604 | HCID 58487604 | — |
Reaction Steps
The mixture of 1-tert-butyl 3-ethyl 3-fluoropiperidine-1,3-dicarboxylate 33 and 1a,b (0.8 g, 0.0029 mol) and acetamide oxime (0.54 g, 0.0073 mol) were dissolved in 30 mL tetrahydrofuran. Sodium methoxide (0.79 g, 0.0146 mol) was added and the mixture was heated at reflux for 1.75 hours. The mixture was concentrated and partitioned between water (25 mL) and ethyl acetate (1×100 mL). The aqueous layer was extracted with an additional 50 mL ethyl acetate. The combined organics were washed with 1×25 mL water, 1×40 mL saturated sodium chloride, and dried over Na2SO4. The dried organics were evaporated to an oil. The residue was chromatographed to remove 1a,b with 15 g silica gel, 100% dichloromethane to 5% ethyl acetate/dichloromethane, to obtain 0.18 g of clear colorless oil. MS (ESI) m/z 324 [M+K]+. 1H NMR (CDCl3) δ 1.45 (s, 9H), 1.55-62 (m, 1H), 1.70-1.74 (d, 1H), 1.92-1.95 (m, 1H), 2.17 (m, 1H), 2.29-2.32 (m, 1H), 2.43 (s, 3H), 3.06-3.12 (m, 1H), 3.89-3.92 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174972B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-a8d082a3e53b4b198af84f5091529e3e |
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| Source note | uspto-grants-2015_11 |
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