HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471748Generated: October 30, 2026
Triphenylphosphine → HCID 86690787, compound
https://huagongshe.com/reaction/1471748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | Methyl 6-(hydroxymethyl)picolinate | HCID 11513809 | — |
| Reactant | HCID 86690788 | HCID 86690788 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86690787 | HCID 86690787 | 60% |
Reaction Steps
Into a 50-mL round-bottom flask, which was purged and maintained with an inert atmosphere of nitrogen, was placed a solution of methyl 6-(hydroxymethyl)pyridine-2-carboxylate (300 mg, 1.79 mmol, 1.00 equiv) in tetrahydrofuran (15 mL). 4-(Dimethoxymethyl)pyridin-3-ol (304.2 mg, 1.80 mmol, 1.00 equiv), and triphenylphosphane (615 mg, 2.34 mmol, 1.30 equiv) was added to the reaction mixture. This was followed by the addition of DIAD (473.1 mg, 2.34 mmol, 1.30 equiv) dropwise at 0° C. The resulting solution was stirred overnight at room temperature, and then it was quenched by the addition of 10 mL of water. The resulting solution was extracted with 2×50 mL of ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:5-1:1) as eluent to yield 340 mg (60%) of methyl 6-([[4-(dimethoxymethyl)pyridin-3-yl]oxy]methyl)pyridine-2-carboxylate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012450B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-3c2b721efd3a43e1b9d4a30afd69942b |
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| Source note | uspto-grants-2015_04 |
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