HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10906Generated: October 29, 2026
Water → 11,12-Dimethylene-13-oxa-tricyclo[7.3.1.01,7]tridecane
https://huagongshe.com/reaction/10906
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | 2-(2-Hydroxy-4-trimethylsilanylmethyl-hexa-4,5-dienyl)-cycloheptanone | HCID 12156685 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 11,12-Dimethylene-13-oxa-tricyclo[7.3.1.01,7]tridecane | HCID 11344739 | 90.2% |
Reaction Steps
1.30 mL of ether was added to 2-(2-hydroxy-4-trimethylsilanylmethyl-hexa-4,5-dienyl)-cycloheptanone (95 mg, 0.32 mmol) under nitrogen atmosphere. While stirring at −78° C., TMSOTf (58.4 μL, 0.32 mmol) was added. While stirring the reaction mixture, the reaction temperature was slowly increased to room temperature for 3 hours. The reaction mixture was stirred at room temperature for 30 minutes. After the reaction was completed, H2O was added. After stirring for about 5 minutes, the reaction mixture was diluted with EtOAc and washed with water and saturated brine. The organic layer was separated from the reaction mixture and dried with anhydrous MgSO4. The solvent was removed under reduced pressure and the remaining material was purified with column chromatography (EtOAc/n-hexane=1/6) to obtain 59 mg of the product (90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094913B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-d98115824bce4000b70e1610633eaced |
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| Source note | uspto-grants-2006_08 |
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