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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602508Generated: November 1, 2026

Isopropanol → 4-Fluoro-1-nitro-2-(propan-2-yloxy)benzene

https://huagongshe.com/reaction/602508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventTetrahydrofuranHCID 8028—
Product4-Fluoro-1-nitro-2-(propan-2-yloxy)benzeneHCID 1063183278%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Fluoro-2-nitrophenol (48 g) was dissolved in dry tetrahydrofuran (THF) (300 mL). Triphenylphosphine (88 g) and 2-propanol (47 mL) were added, and the resulting mixture was cooled to 0° C. Diisopropylazodicarboxylate (66 mL) was added dropwise. The resulting mixture was allowed to warm to room temperature and stirred over night. The solvent was evaporated in vacuo and the resulting mixture was filtered through silica (heptane/ethyl acetate 1:1). The solvent was evaporated in vacuo and the resulting mixture was recrystallised from heptane/ethyl acetate (1:1). The organic phase was separated from the crystalline solid by filtration, the solvent was evaporated in vacuo, and the remaining product was purified by flash chromatography (silica gel, heptane/ethyl acetate 9:1), yielding the title compound as colourless oil (47.2 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906537B2
Source datasetuspto-grants-2011_03
ORD IDord-3355035c52ff4b1190983c389afc4ba7
Source noteuspto-grants-2011_03