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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730968Generated: October 30, 2026

5H-Dibenzo[a,d]cyclohepten-5-one → HCID 12690612, compound

https://huagongshe.com/reaction/1730968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5H-Dibenzo[a,d]cyclohepten-5-oneHCID 16679—
ReactantSodium hydrideHCID 24758—
ReactantTrimethylsulfonium iodideHCID 75127—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12690612HCID 12690612—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 4.6 g. of sodium hydride (57%) and 100 ml. of dimethylsulfoxide is heated under nitrogen at 75° C. for 50 minutes and the resulting mixture treated by addition of 40 ml. tetrahydrofuran and then cooled to 0° C. Over a period of 3 minutes there is then added 10.2 g. of trimethylsulfonium iodide in 100 ml. of dimethylsulfoxide, the resulting mixture stirred for one minute and there is then added over a period of 10 minutes a solution of 16.4 g. of dibenzo[a,d]cyclo-hepten-5-one in 40 ml. of tetrahydrofuran. The resulting mixture is kept overnight at temperature of 5° C. and then stirred for 3 hours at room temperature (20° C.). The mixture is then poured onto 3 times its volume of ice water, extracted twice each with 600 ml. of pentane, the organic phases combined, washed four times with water, dried over anhydrous sodium sulfate and evaporated in vacuo to crystallize spiro[dibenzo[ a,d] cycloheptene-5,2'-oxirane], m.p. 90°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994918
Source datasetuspto-grants-1976_11
ORD IDord-34ae04364bd64bcd83c60b43ba4aa656
Source noteuspto-grants-1976_11