HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894221Generated: October 31, 2026
2-Cyano-6,11-dihydro-11-oxodibenz[b,e]oxepin → 2-Cyano-6,11-dihydro-11-ethylidenedibenz[b,e]oxepin
https://huagongshe.com/reaction/894221
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Cyano-6,11-dihydro-11-oxodibenz[b,e]oxepin | HCID 12446825 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Catalyst | Phosphonium, ethyltriphenyl-, bromide (1:1) | HCID 73727 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Cyano-6,11-dihydro-11-ethylidenedibenz[b,e]oxepin | HCID 53673425 | — |
Reaction Steps
Suspent 23.6 gm of ethyl triphenylphosphonium bromide in 200 ml of dry tetrahydrofuran add dropwise 2.4 ml of t-butyllithium in hexane with stirring at room temperature under a nitrogen atmosphere. Continue stirring for 3 hours and then cool to -70° C. in a dry ice bath. Add 10 gm. of 2-cyano-6,11-dihydro-11-oxodibenz[b,e]oxepin in 75 ml of dry tetrahydrofuran dropwise over 30 minutes. Continue stirring at -70° C. for 30 minutes, warm to room temperature and continue stirring overnight under a nitrogen atmosphere. Pour the mixture into 400 ml. of ether, filter and wash the filtrate with saturated aqueous sodium chloride solution. Dry over anhydrous magnesium sulfate and strip to dryness. Chromatograph the residue over silica gel, eluting with 5% ethyl acetate in hexane to obtain the final product (5.73 gm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04282365 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-080c06b0d92e4e499148774c4771fca7 |
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| Source note | uspto-grants-1981_08 |
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