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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Lithium acetate | HCID 3474584 | — |
| Reactant | (E)-(3,7-Difluoro-6H-dibenzo[b,e]oxepin-11-ylidene)-acetic acid ethyl ester | HCID 67335842 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (E)-11-Bromomethylene-3,7-difluoro-6,11-dihydro-dibenzo[b,e]oxepine | HCID 67334731 | 89.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994164B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4441852ac2414936ba61ed694622d3b0 |
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| Source note | uspto-grants-2011_08 |
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