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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528603Generated: October 25, 2026

Sodium hydride → 2-(6-fluoro-2H-benzo[b][1,4]oxazin-4(3H)-yl)-5-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/528603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Fluoro-5-(trifluoromethyl)benzonitrileHCID 521016—
Reactant6-Fluoro-3,4-dihydro-2H-1,4-benzoxazineHCID 16244459—
Product2-(6-fluoro-2H-benzo[b][1,4]oxazin-4(3H)-yl)-5-(trifluoromethyl)benzonitrileHCID 8976207028.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 250 ml round bottom flask charged with 6-fluoro-3,4-dihydro-2H-benzo[b][1,4]oxazine (5.00 g, 32.6 mmol) was dried under high vacuum and placed under nitrogen prior to the addition of THF (131 ml). The solution was cooled in an ice water bath for 10 mins prior to the addition of sodium hydride (60% in mineral oil) (1.436 g, 35.9 mmol), added carefully in two portions 5 mins apart. The resulting suspension was stirred for 15 min at 0° C. then 90 min at room temp yielding a brownish suspension. To the suspension was added 2-fluoro-5-(trifluoromethyl)benzonitrile (6.79 g, 35.9 mmol) at room temperature. The mixture was stirred at 60° C. overnight affording about 75% conversion according to LC-MS. The dark solution was cooled in an ice water bath and carefully added to a stirred flask of water/ice/NH4Cl which was extracted with EtOAc (2×). The combined organics were dried with Na2SO4, filtered, and dried under reduced pressure. The crude residue was purified with a 120 g ISCO gold column (load column loaded with crude brown oil directly with DCM rinsing) ramping EtOAc in heptane (0-25%, then isocratic at 25%) providing product cleanly (3.65 g, yellow solid) as well as a large portion which coeluted with starting amine and other minor impurities. The mixture was dried under reduced pressure and passed through a 25 g SCX-2 column, then a second 25 g SCX-2 column since after the first wash some dark materials eluted through. DCM was used as the eluent providing 2-(6-fluoro-2H-benzo[b][1,4]oxazin-4(3 H)-yl)-5-(trifluoromethyl)benzonitrile as a tan solid (3.0 g) (6.65 g total, 63%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 3.84-3.91 (m, 2 H) 4.26-4.31 (m, 2 H) 6.53 (dd, J=9.93, 2.89 Hz, 1 H) 6.64 (ddd, J=9.00, 7.82, 2.93 Hz, 1 H) 6.90 (dd, J=8.95, 5.33 Hz, 1 H) 7.55 (d, J=8.71 Hz, 1 H) 7.76 (ddd, J=8.71, 2.25, 0.59 Hz, 1H) 7.95 (dd, J=1.57, 0.68 Hz, 1 H). m/z (ESI) 323.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346798B2
Source datasetuspto-grants-2016_05
ORD IDord-41e55818566e43889e9de6de1e1a8dbd
Source noteuspto-grants-2016_05