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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648224Generated: November 2, 2026

1-Nitropropane → Benzene, 1-fluoro-2-(2-nitro-1-buten-1-yl)-

https://huagongshe.com/reaction/1648224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NitropropaneHCID 7903—
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantSodium BicarbonateHCID 516892—
ReactantAmmonium AcetateHCID 517165—
SolventAcetic AcidHCID 176—
ProductBenzene, 1-fluoro-2-(2-nitro-1-buten-1-yl)-HCID 422610799.5%

Reaction Steps

30 ml of acetic acid were added to 4.73 g (38.11 mmole) of 2-fluorobenzaldehyde, 4.41 g (49.49 mmole) of nitropropane and 3.23 g (41.90 mmole) of ammonium acetate, and the resulting mixture was heated under reflux, whilst stirring, for 4 hours. At the end of this time, the reaction mixture was cooled to room temperature, neutralized with an aqueous solution of sodium hydrogencarbonate and extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate, and then xylene was added to the solution. The mixture was concentrated by evaporation under reduced pressure, to give 7.4 g of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436242
Source datasetuspto-grants-1995_07
ORD IDord-8a20029a5bb544398c0a525a16f71cec
Source noteuspto-grants-1995_07