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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173059Generated: November 1, 2026

Nitric Acid → 1-((1R,5S,6R)-6-(4-nitro-phenyl)-3-aza-bicyclo[3.2.0]hept-3-yl)-propan-1-one

https://huagongshe.com/reaction/1173059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
Reactant1-((1R,5S,6R)-6-Phenyl-3-aza-bicyclo[3.2.0]hept-3-yl)-propan-1-oneHCID 67365159—
SolventWaterHCID 962—
SolventNitromethaneHCID 6375—
Product1-((1R,5S,6R)-6-(4-nitro-phenyl)-3-aza-bicyclo[3.2.0]hept-3-yl)-propan-1-oneHCID 67364849106.2%

Reaction Conditions

Temperature-8 °C

Reaction Steps

1.0 g of 1-((1R,5S,6R)-6-Phenyl-3-aza-bicyclo[3.2.0]hept-3-yl)-propan-1-one (4.36 mmol) were dissolved in 12 ml of nitromethane. At −8° C., a mixture of 0.3 ml of nitric acid (65%, 4.36 mmol) and 4.6 ml of sulphuric acid (95%) in 0.76 ml of water were added dropwise within 45 minutes. Stirring at −8° C. was continued for 30 minutes, before 20 ml of ice water were added and the aqueous phase was extracted twice with diethyl ether, the combined organic layers were dried over magnesium sulfate, filtered, and the solvent was evaporated under reduced pressure to yield 1.27 g of the product as a mixture of 2:1 para versus ortho substituted product which was used without further separation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834048B2
Source datasetuspto-grants-2010_11
ORD IDord-7720f66765ac45a2af1becf64bacf3f4
Source noteuspto-grants-2010_11