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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670594Generated: November 2, 2026

Acetic Acid → (e)-11-(Bromomethylene)-3-fluoro-6,11-dihydrodibenzo[b,e]oxepine

https://huagongshe.com/reaction/1670594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantLithium HydroxideHCID 3939—
ReactantN-bromobutanimideHCID 67184—
Reactant(3-fluoro-6H-dibenzo[b,e]oxepin-11-ylidene)-acetic acid ethyl esterHCID 67134827—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product(e)-11-(Bromomethylene)-3-fluoro-6,11-dihydrodibenzo[b,e]oxepineHCID 5946868493.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a suspension of (3-fluoro-6H-dibenzo[b,e]oxepin-11-ylidene)-acetic acid ethyl ester (0.23 mol, 69.5 g) in isopropanol (725 mL) add a solution of lithium hydroxide (0.53 mol, 12.0 g) in water (125 mL) and warm to 70° C. for 4 h. Allow the mixture to cool to 40° C. and then treat with glacial acetic acid (0.44 mol, 25 mL). After stirring for 15 min, add N-bromosuccinimide (0.25 mol, 44 g). Bubbling ensues, the temperature rises to 45° C., and solids form after a few min. Stir the mixture at 40-45° C. for one hour and cool to room temperature. Add sodium bisulfite (4.5 g) in water (150 mL), saturated aqueous sodium bicarbonate (150 mL), and water (450 mL). Filter the resulting suspension and rinse with cold 1:1 isopropanol/water (300 mL). Dry the solid at 60° C./20 mm Hg overnight to obtain the title compound (65.8 g, 93%). 1H NMR (400 MHz, DMSO-d6) δ 4.9-5.4 (br d, 2H), 6.63 (dd, 1H), 6.77 (dt, 1H), 7.13 (s, 1H), 7.32-7.46 (m, 4H), 7.52 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994164B2
Source datasetuspto-grants-2011_08
ORD IDord-33770e04adf94df7896d41ee3356ed3c
Source noteuspto-grants-2011_08