Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 68462653 | HCID 68462653 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68461294 | HCID 68461294 | — |
Reaction Steps
2.0 g of methyl 4-methoxy-pyridin-2,6-dicarboxylic acid (compound E3) are suspended in 40 ml of dioxane and 5.63 ml of tert-butanol. 2.63 ml of triethylamine and 4.08 ml of diphenylphosphoryl azide are added to the mixture. Subsequently, the reaction mixture is heated at 80° C. for 72 h with vigorous stirring under a nitrogen atmosphere. Further 0.41 ml each of diphenylphosphoryl azide are added after 24 h and 48 h, respectively. Thereafter, the mixture is cooled to room temperature, diluted with 300 ml of ethyl acetate and extracted four times each with 80 ml of sat sodium hydrogencarbonate. The organic layer is dried using sodium sulphate, filtered with suction and concentrated in vacuum. The crude product (5.08 g) is purified by chromatography (eluent: toluene/ethyl acetate 5:1) to afford 1.10 g of the title compound as a colorless oil. TSP-MS: 283.1 [MH+]. TLC: Rf=0.24 (toluene/ethyl acetate 5:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07317021B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-d1b30fbb4af14b2daa1e72d0e6a97637 |
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| Source note | uspto-grants-2008_01 |
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