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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551610Generated: October 26, 2026

Nitromethane → Tert-butyl[(1s,5r,6r)-6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetate

https://huagongshe.com/reaction/551610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantTert-butyl(+/-)-(1s,5r)bicyclo[3.2.0]hept-3-en-6-ylideneacetateHCID 90739074—
SolventHydrochloric AcidHCID 313—
ProductTert-butyl[(1s,5r,6r)-6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetateHCID 91600480—

Reaction Steps

Tert-butyl(±)-(1S,5R)bicyclo[3.2.0]hept-3-en-6-ylideneacetate (1.73 g, 8.39 mmol) was dissolved in nitromethane (10 mL). To the solution, 1,8-diazabicyclo[5.4.0]undec-7-ene (1.3 mL, 8.4 mmol) was added, and the mixture was stirred at room temperature for 1 hour and then heated with stirring at 50 to 60° C. for 5 hours. The mixture was allowed to cool and then diluted with 1 N hydrochloric acid and saturated saline, followed by extraction with ethyl acetate. Then, the organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to obtain the compound of interest as a colorless oil substance (1.98 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947738B2
Source datasetuspto-grants-2011_05
ORD IDord-019a5182c412469494ead2ee2ef3562e
Source noteuspto-grants-2011_05