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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyano-6,11-dihydro-11-oxodibenz[b,e]oxepinHCID 12446825—
ReactantHCID 178418306HCID 178418306—
CatalystPhosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-Cyano-6,11-dihydro-11-ethylidenedibenz[b,e]oxepinHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04282365
Source datasetuspto-grants-1981_08
ORD IDord-080c06b0d92e4e499148774c4771fca7
Source noteuspto-grants-1981_08