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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402901Generated: October 30, 2026

Dimethylformamide → HCID 89558427, compound

https://huagongshe.com/reaction/2402901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Bromo-5-fluorobenzotrifluorideHCID 520983—
ReactantSodium t-butoxideHCID 23676156—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 89558427HCID 8955842799.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 2.4 M solution of sodium-tert-butoxide in THF (156.3 mL, 375 mmol, Chemetall) was added DMF (38.5 mL, 500 mmol) and then 2,2,2-trifluoroethanol (41.27 g, 413 mmol). After the addition of 2-bromo-5-fluorobenzotrifluoride (60.8 g, 250 mmol) the reaction mixture was heated to reflux and stirred at ˜80° C. for 7 h. After cooling to 25° C., TBME (800 mL) was added and the reaction mixture was washed with 1M HCl (400 mL), 5% NaHCO3 (400 mL) and 10% brine (400 mL). The organic layer was dried (Na2SO4), filtered and evaporated to dryness (60° C./≧5 mbar), affording the crude title product (80.0 g, 99.1%) as a yellow oil which was used without purification in the next step 1H NMR (CDCl3, 400 MHz) δ 4.38 (q, J=7.9 Hz, 2H), 6.98 (dd, J1=8.6 Hz, J2=2.7 Hz, 1H), 7.28 (d, J=2.7 Hz, 1H), 7.65 (d, J=8.9 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796471B2
Source datasetuspto-grants-2014_08
ORD IDord-4bdeaa3638f54a99a2b59b6733e41bae
Source noteuspto-grants-2014_08