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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708124Generated: October 25, 2026

Tosylmethyl isocyanide → 3-Chloro-8-methyl-2-(5-oxazolyl)-8-azabicyclo[3.2.1]oct-2-ene oxalate

https://huagongshe.com/reaction/1708124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTosylmethyl isocyanideHCID 161915—
Reactant3-Chloro-2-formyl-8-methyl-8-azabicyclo[3.2.1]oct-2-ene oxalateHCID 18960838—
SolventMethanolHCID 887—
Product3-Chloro-8-methyl-2-(5-oxazolyl)-8-azabicyclo[3.2.1]oct-2-ene oxalateHCID 18960936—

Reaction Steps

To a solution of 3-chloro-2-formyl-8-methyl-8-azabicyclo[3.2.1]oct-2-ene oxalate (0.55 g, 2 mmol) in 20 ml methanol powdered potassium carbonate (1.5 g) and tosylmethylisocyanide (0.4 g, 2 mmol) was added. The reaction mixture was stirred at room temperature for 2 h. Upon evaporation in vacuo water (30 ml) was added to the residue and the water solution extracted with methylenechloride (3×20 ml). The combined methylenechloride extracts were dried and evaporated in vacuo. The residue was dissolved in ethanol, and the title compound precipitated with a 1M oxalic acid ether solution. The compound was filtered and dried. M.p. 69°-71° C. decomposes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356912
Source datasetuspto-grants-1994_10
ORD IDord-a5071ff4ae814bba8a755e455789ee29
Source noteuspto-grants-1994_10