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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5H-Dibenzo[a,d]cyclohepten-5-one | HCID 16679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12690612 | HCID 12690612 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03994918 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-34ae04364bd64bcd83c60b43ba4aa656 |
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| Source note | uspto-grants-1976_11 |
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