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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantTrimethylsilyl triflateHCID 65367—
Reactant2-(2-Hydroxy-4-trimethylsilanylmethyl-hexa-4,5-dienyl)-cycloheptanoneHCID 12156685—
SolventEthyl AcetateHCID 8857—
Product11,12-Dimethylene-13-oxa-tricyclo[7.3.1.01,7]tridecaneHCID 1134473990.2%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094913B2
Source datasetuspto-grants-2006_08
ORD IDord-d98115824bce4000b70e1610633eaced
Source noteuspto-grants-2006_08