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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838063Generated: November 2, 2026

2-Nitrobenzaldehyde → HCID 15673275, compound

https://huagongshe.com/reaction/1838063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrobenzaldehydeHCID 11101—
ReactantEthyl bromodifluoroacetateHCID 69585—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 15673275HCID 1567327591%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a slurry of activated zinc (6.25 g, 99.2 mmol) in 75 mL anhydrous THF, was added ethyl bromodifluoroacetate (11.0 mL, 85.8 mmol) and the mixture was heated to reflux. After a visible reaction had occurred, 2-nitrobenzaldehyde (5.0 g, 33.1 mmol) in 30 mL anhydrous THF, was added dropwise to maintain reflux. After 3 h, the solution was cooled to 23° C., diluted with EtOAc (50 mL), washed with 1M KHSO4 (2×50 mL) and brine (1×50 mL), and dried (Na2SO4). Concentration in vacuo yielded a residue which was purified by flash chromatography (chloroform:EtOH, 99:1) to afford 2-(3-ethoxy-3-oxo-2,2-difluoro-1-hydroxypropyl)nitrobenzene (8.28 g, 91%) as an orange oil, which was taken on to the next step without further characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673784B1
Source datasetuspto-grants-2004_01
ORD IDord-6687db08db43423eaf82381646a18a82
Source noteuspto-grants-2004_01