HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234583Generated: October 30, 2026
Sodium Hydroxide → HCID 23354809, compound
https://huagongshe.com/reaction/234583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 23354782 | HCID 23354782 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23354809 | HCID 23354809 | 52.7% |
Reaction Steps
Then, 0.40 g (0.88 mM) of 2-oxooctyl-(6-decyloxy-2-naphthoyl)amine, 0.38 g (0.94 mM) of Lawesson's reagent and 6 ml of tetrahydrofuran were placed in a 30 ml-round-bottomed flask, followed by heat-refluxing for 45 minutes under stirring. After the reaction, the reaction mixture was poured into a solution of 0.27 g of sodium hydroxide in 70 ml of 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. The residue was purified by silica gel column chromatography (eluent: toluene/hexane=1/1) and recrystallized from a mixture solvent of acetonemethanol to obtain 0.21 g of 2-(6-decyloxy-2-naphthyl)-5-hexylthiazole (Yield: 52.7%). ##STR236##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05595685 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-047a01c63ee84cc0a39837d7f79c1398 |
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| Source note | uspto-grants-1997_01 |
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