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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705689Generated: October 29, 2026

N-Hydroxyacetamidine → HCID 58487604, compound

https://huagongshe.com/reaction/705689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyacetamidineHCID 30926—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 49761218HCID 49761218—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58487604HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174972B2
Source datasetuspto-grants-2015_11
ORD IDord-a8d082a3e53b4b198af84f5091529e3e
Source noteuspto-grants-2015_11