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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670600Generated: October 30, 2026

Sodium Hydroxide → (E)-11-Bromomethylene-3,7-difluoro-6,11-dihydro-dibenzo[b,e]oxepine

https://huagongshe.com/reaction/1670600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium acetateHCID 3474584—
Reactant(E)-(3,7-Difluoro-6H-dibenzo[b,e]oxepin-11-ylidene)-acetic acid ethyl esterHCID 67335842—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(E)-11-Bromomethylene-3,7-difluoro-6,11-dihydro-dibenzo[b,e]oxepineHCID 6733473189.2%

Reaction Steps

Heat a stirred slurry of (E)-(3,7-difluoro-6H-dibenzo[b,e]oxepin-11-ylidene)-acetic acid ethyl ester (601 mmol, 190 g) in methanol (1.9 L) and 5 N sodium hydroxide (1.20 mol, 240 mL) to 50° C. for 2 h. Remove the methanol in vacuo and reslurry the resulting black sludge in water (3 L). Add 5 N hydrochloride acid (250 mL) over 45 min, stir for 2.5 h, filter, and rinse the residue with water (4×200 mL). Dry the gray solid in vacuo at 60° C. overnight, and 80° C. for 6 h. Dissolve the solid (still wet, contains approximately 95 g of water) and lithium acetate (60.1 mmol, 4 g, 0.1 eq) in acetonitrile (1.7 L) and stir for 15 min. Add N-bromosuccinimide (661 mmol, 118 g) in one portion and stir for 2.5 h. Add 0.25 M sodium thiosulfate (400 mL), followed by saturated aqueous sodium bicarbonate (400 mL), and water (900 mL). Stir the mixture for one hour at room temperature and then stir for 2 h on an ice bath. Filter the mixture and rinse with cold acetonitrile (300 mL). Dry overnight in vacuo at 50° C. to obtain the title compound as a light beige solid (173.3 g, 89%). 1H NMR (DMSO-d6) δ 5.25 (s, 2H), 6.67 (dd, 1H), 6.81 (dt, 1H), 7.20 (s, 1H), 7.22 (d, 1H), 7.28 (t, 1H), 7.36 (dd, 1H), 7.48 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994164B2
Source datasetuspto-grants-2011_08
ORD IDord-4441852ac2414936ba61ed694622d3b0
Source noteuspto-grants-2011_08