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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597987Generated: October 30, 2026

Aldoxime → HCID 57486351, compound

https://huagongshe.com/reaction/597987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAldoximeHCID 7863—
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 57485790HCID 57485790—
CatalystPyridineHCID 1049—
SolventChloroformHCID 6212—
ProductHCID 57486351HCID 57486351—

Reaction Steps

To a solution of acetaldoxime (65 mg, 1.1 mmol) in 15 mL of chloroform were added 2 drops of pyridine, followed by N-chlorosuccinimide (146 mg, 1.1 mmol). After stirring the cloudy mixture for 1 h at ambient temperature, tert-butyl 4-ethynyl-6-azabicyclo[3.2.1]oct-3-ene-6-carboxylate (233 mg, 1.00 mmol) was added in 2 mL of chloroform, followed by drop-wise addition of triethylamine (0.175 mL, 1.25 mmol). The mixture was stirred at ambient temperature for 4 h and then concentrated to dryness under reduced pressure. The residue was chromatographed on a silica gel column, with a gradient of 2:1 hexane/ethyl acetate to 2:1 ethyl acetate/hexane, to give first recovered starting material, then tert-butyl 4-(3-methyl-5-isoxazolyl)-6-azabicyclo[3.2.1]oct-3-ene-6-carboxylate (100 mg, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897611B2
Source datasetuspto-grants-2011_03
ORD IDord-95d31f415d3d4010a6b6dacdd40d7fea
Source noteuspto-grants-2011_03