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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190981Generated: November 1, 2026

Nitromethane → Tert-butyl [6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetate

https://huagongshe.com/reaction/2190981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantTert-butyl bicyclo[3.2.0]hept-3-en-6-ylideneacetateHCID 66697018—
SolventHydrochloric AcidHCID 313—
ProductTert-butyl [6-(nitromethyl)bicyclo[3.2.0]hept-3-en-6-yl]acetateHCID 66803873—

Reaction Steps

Tert-butyl 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 numberUS08324425B2
Source datasetuspto-grants-2012_12
ORD IDord-c377fd099a4041939f8a3c4af58f0efb
Source noteuspto-grants-2012_12