HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838063Generated: November 2, 2026
2-Nitrobenzaldehyde → HCID 15673275, compound
https://huagongshe.com/reaction/1838063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15673275 | HCID 15673275 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06673784B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-6687db08db43423eaf82381646a18a82 |
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| Source note | uspto-grants-2004_01 |
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