Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isophthaloyl chloride | HCID 7451 | — |
| Reactant | HCID 67315563 | HCID 67315563 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 59236812 | HCID 59236812 | 67% |
Reaction Steps
2.0 g of 6-(2H-tetrazol-5-yl)-2,2′:6′2″-terpyridine was dissolved in 50 ml of dehydrated pyridine. Temperature was elevated to 120° C., and 30 ml was dehydrated by azeotropy. After cooling to 50° C., 0.68 g of isophthaloyl dichloride was added. Temperature was elevated to 110° C., and stirring was conducted for 3 hours under flux. After cooling to room temperature, the reaction solution was poured into 200 ml water, and a precipitated yellowish-brown solid was taken out by suction filtration, and washed with water. The solid obtained was vacuum dried at 80° C. for 20 hours, and purified with adsorption purification (carrier: NH silica gel, eluting solution: chloroform) to obtain 1.53 g (yield 67%) of TpyOXDm. The product was identified with NMR analysis. The result of NMR analysis (CDCl3) was as follows. 9.12 ppm (1H), 8.85 ppm (2H), 8.62-8.73 ppm (6H), 8.37-8.51 ppm (6H), 7.79-8.12 ppm (7H), 7.35 ppm (2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977671B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-f91282ee3be844ff938bf9361c75aa27 |
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| Source note | uspto-grants-2011_07 |
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