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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551663Generated: October 28, 2026

Nitromethane → HCID 131728910, compound

https://huagongshe.com/reaction/551663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantHCID 91368801HCID 91368801—
ProductHCID 131728910HCID 131728910—

Reaction Conditions

Temperature55 °C

Reaction Steps

Tert-butyl(±)-(1S,5R)-3-allylbicyclo[3.2.0]hept-3-en-6-ylideneacetate (0.63 g, 2 mmol) was dissolved in nitromethane (5 mL). To the solution, 1,8-diazabicyclo[5.4.0]undec-7-ene (0.45 mL, 3 mmol) was added, and the mixture was heated with stirring at 50 to 60° C. for 7 hours. The mixture was allowed to cool, and a saturated aqueous solution of potassium dihydrogen phosphate was then added thereto, 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 (367.0 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947738B2
Source datasetuspto-grants-2011_05
ORD IDord-5ffe092995e34df5aa7d96681d811435
Source noteuspto-grants-2011_05