HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249219Generated: October 31, 2026
Benzyltrimethylammonium hydroxide → 2-Octyl-7-(5-hexyl-1,3,4-thiadiazole-2-yl)fluorenone
https://huagongshe.com/reaction/249219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | 2-Octyl-7-(5-hexyl-1,3,4-thiadiazole-2-yl)fluorene | HCID 19760662 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Octyl-7-(5-hexyl-1,3,4-thiadiazole-2-yl)fluorenone | HCID 67885904 | 53.3% |
Reaction Steps
To a solution of 0.20 g (0.45 mM) of 2-octyl-7-(5-hexyl-1,3,4-thiadiazole-2-yl)fluorene in 20 ml of pyridine, 0.27 ml of 40%-trimethylbenzylammonium hydroxide aqueous solutions as added at 3.5°-4.5° C. under stirring on ice water bath, followed by stirring for 0.5 hour at 3.5°-4.5° C. After the reaction, the reaction mixture was poured into ice water to precipitate a crystal. The crystal was recovered by filtration, washed with water and dissolved in toluene, followed by drying with anhydrous sodium sulfate and distilling-off of the solvent under reduced pressure to obtain a residue. The residue was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=20/1) and recrystallized from a mixture solvent of toluene-acetone to obtain 0.11 g of 2-octyl-7-(5-hexyl-1,3,4-thiadiazole-2-yl)fluorenone (Yield: 53.3%). ##STR89##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05213709 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-f43a152c0c8f49e49bf27c325b8742da |
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| Source note | uspto-grants-1993_05 |
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