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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant2-Octyl-7-(5-hexyl-1,3,4-thiadiazole-2-yl)fluoreneHCID 19760662—
SolventPyridineHCID 1049—
Product2-Octyl-7-(5-hexyl-1,3,4-thiadiazole-2-yl)fluorenoneHCID 6788590453.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05213709
Source datasetuspto-grants-1993_05
ORD IDord-f43a152c0c8f49e49bf27c325b8742da
Source noteuspto-grants-1993_05