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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600211Generated: October 25, 2026

Hydroxylamine → HCID 178472247, compound

https://huagongshe.com/reaction/600211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantDiethyl acetylenedicarboxylateHCID 69803—
Reactant1-(2-Trimethylsilanyloxyethoxy)cyclobutanecarbonitrileHCID 57426435—
SolventEthanolHCID 702—
ProductHCID 178472247HCID 178472247—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 1-(2-trimethylsilanyloxyethoxy)cyclobutanecarbonitrile (3.5 g, 16.4 mmol) and 50% aqueous hydroxylamine (1.08 g, 16.4 mmol) in EtOH (16 mL) was stirred in an oil bath heated at 80° C. for 2.5 hrs and then cooled to room temperature. To a solution was added drop-wise diethyl acetylenedicarboxylate (2.93 g, 17.2 mmol) in an ice-bath and the mixture stirred at room temperature for 5 hrs. This mixture was concentrated under vacuum to obtain 6.16 g of a crude brownish oil containing intermediate 21: 1H NMR (500 MHz, CDCl3) δ: 1.19-1.38 (6H, m) 1.72-1.86 (2H, m) 2.06-2.24 (2H, m) 2.29-2.49 (2H, m) 3.26-3.38 (2H, m) 3.63-376 (2H, m) 4.11-4.19 (2H, m) 4.24-4.38 (2H, m) 5.67 (0.25H, s) 5.85 (0.5H, s). HRMS (M+H) calcd for C15H25N2O7: 345.1662; found: 345.1648.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902182B2
Source datasetuspto-grants-2011_03
ORD IDord-b654236f18fc4456aecd3400ffa34a06
Source noteuspto-grants-2011_03