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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745897Generated: October 31, 2026

Dimethylformamide → HCID 22227324, compound

https://huagongshe.com/reaction/1745897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-Bromo-4-[(trifluoroethenyl)oxy]benzeneHCID 2757197—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
ProductHCID 22227324HCID 22227324—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Compound 32 intermediates: To a solution of 4-(trifluorovinyloxy)-bromobenzene (9.25 g, 36.6 mmol) in dry diethyl ether (60 mL) at −78° C. was added t-BuLi (23.7 mL, 1.7 M in pentane) dropwise. One hour later, DMF (4.3 mL, 1.5 eq) was added dropwise. The reaction mixture was stirred at −78° C. for 1 h. Then the reaction mixture was allowed to warm up to room temperature for about 45 min, and quenched by adding water (10 mL). The ethereal layer was collected and the aqueous layer was extracted with diethyl ether. The combined organic layer was washed with water twice (50 mL×2), and dried over sodium sulfate. After filtration and evaporation of the solvent, the product was dried in vacuum overnight to give 4-(trifluorovinyloxy)benzaldehyde as yellow oil, which can be used in next step without further purification. 1H NMR (CDCl3): δ 10.18 (s, 1H), 7.85 (d, J=8.8 Hz, 2H), 7.17 (d, J=8.8 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019453B2
Source datasetuspto-grants-2006_03
ORD IDord-b8041665613b402fbb247493797aa88f
Source noteuspto-grants-2006_03