HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733389Generated: October 31, 2026
Ethanol → 9-(8-Aza-bicyclo[3.2.1]oct-3-yl)-9H-xanthene-3-carboxylic acid diethylamide
https://huagongshe.com/reaction/733389
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 9-(8-azabicyclo[3.2.1]octan-3-ylidene)-N,N-diethylxanthene-3-carboxamide | HCID 46918141 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 9-(8-Aza-bicyclo[3.2.1]oct-3-yl)-9H-xanthene-3-carboxylic acid diethylamide | HCID 11516656 | — |
Reaction Steps
To a solution of 9-(8-aza-bicyclo[3.2.1]oct-3-ylidene)-9H-xanthene-3-carboxylic acid diethylamide, 8a (3 g, 7.7 mmol) in chloroform (50 mL) were added ethanol (2.25 mL, 38.6 mmol) and trimethylsilyl iodide (5.25 mL, 38.6 mmol). The mixture was stirred at 100° C. for 2 h in a sealed tube. The reaction was allowed to cool to rt and washed with 1 N NaOH, aqueous Na2S2O4, and brine. The organic phase was dried over sodium sulfate, filtered, and concentrated, to yield title compound 9-(8-aza-bicyclo[3.2.1]oct-3-yl)-9H-xanthene-3-carboxylic acid diethylamide, 9a (3.0 g, 0.53 mmol). MS m/z=391.4 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589104B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-347a6090a9414b3380375744e7b78a00 |
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| Source note | uspto-grants-2009_09 |
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