Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Iodohexane | HCID 12527 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 15027123 | HCID 15027123 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15027124 | HCID 15027124 | 32.5% |
Reaction Steps
To a solution of 0.40 g (1.10 mM) of 2-(4-octylphenyl)-5-(4-hydroxyphenyl)thiazole in 20 ml of N,N-dimethylformamide (DMF), 0.40 g (1.10 mM) of potassium hydroxide was added, followed by stirring for 45 minutes at 100° C. To the mixture, 0.36 g (1.70 mM) of hexyl iodide was added at 100° C. under stirring, followed by further stirring for 6 hours and 16 minutes at 120° C. After the reaction, the reaction mixture was poured into 100 ml of water and extracted with ethyl acetate. The organic layer was washed with water, 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) and recrystallized from ethanol to obtain 0.16 g of 2-(4-octylphenyl)-5-(4-hexyloxyphenyl)thiazole (Yield: 32.3%). ##STR43##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05269964 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-5e2af2e411994d0b8e543ffa5afba457 |
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| Source note | uspto-grants-1993_12 |
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