Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | 1,3,5-Triazine | HCID 9262 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 135838255 | HCID 135838255 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 135609944 | HCID 135609944 | — |
Reaction Steps
To a 500 mL round bottomed flask equipped with a magnetic stirrer, condenser and nitrogen atmosphere are charged 2.0 g (4.2 mmol) of 2,4-bis-(2,4-dihydroxyphenyl)-6-[4-(phenylthio)phenyl]-s-triazine, 0.58 g (4.2 mmol) of potassium carbonate and 30 mL of N,N-dimethylformamide. The mixture is heated to 90° C., and the s-triazine compound dissolves readily. Bromobutane (4.5 mL, 42.0 mmol) is added all at once. The reaction mixture is heated at 90° C. for 2.5 hours and then stirred at room temperature overnight yielding a yellow precipitate. Chilled water is added and the yellow precipitate is isolated by vacuum filtration to give 2.74 g of crude product. The crude product is purified by flash chromatography with 1:1 heptane:ethyl acetate to afford 0.26 g (10%) yield of the title compound as a yellow solid; mp>250°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05476937 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-772c83da69214f39be12384f9f82a647 |
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| Source note | uspto-grants-1995_12 |
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