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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75726Generated: October 25, 2026

Hydroxylamine → HCID 178472246, compound

https://huagongshe.com/reaction/75726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantDiethyl acetylenedicarboxylateHCID 69803—
ReactantBenzyl 1-cyano-4-fluoro-4-(hydroxymethyl)cyclohexylcarbamateHCID 67977046—
SolventEthanolHCID 702—
ProductHCID 178472246HCID 17847224660.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A flask was charged with benzyl 1-cyano-4-fluoro-4-(hydroxymethyl)cyclohexylcarbamate, Intermediate 33, (13.0 g, 42.4 mmol), EtOH (100 mL) and aqueous hydroxylamine (26.0 mL, 424 mmol). The reaction was stirred at 80° C. under nitrogen for 2 hours. The mixture was concentrated and the resulting residue diluted with CH2Cl2, washed with brine, dried (MgSO4) and the solvent evaporated to provide a colorless oil. The oil was dissolved in EtOH (100 mL) to which diethyl acetylenedicarboxylate (13.54 mL, 85 mmol) was added. The reaction was stirred under nitrogen for one hour. The solution was concentrated and the residue was dissolved in CH2Cl2 then purified by silica gel column chromatography eluting with hexane/ethyl acetate (0 to 100%). The appropriate fractions were combined and evaporated to give the title compound (13.01 g, 25.5 mmol, 60.2% yield)] as a light yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835411B2
Source datasetuspto-grants-2014_09
ORD IDord-84c4207b97494f619cee774f0d6465ba
Source noteuspto-grants-2014_09