Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 68871844 | HCID 68871844 | — |
| Product | HCID 68873141 | HCID 68873141 | 12% |
Reaction Steps
To a solution of 5-bromo-2-dimethylamino-4-ethoxy-benzonitrile (1.95 g, 7.3 mmol) in 7.25 mL of dioxane was added sodium methoxide (581 mg, 10.77 mmol), methyl formate (1.85 mL, 30 mmol), and trans-dichlorobis(triphenylphosphine) palladium(II) (281 mg, 0.4 mmol). The mixture was agitated by bubbling nitrogen gas through the solution. To the opening of the vial is affixed a balloon. The reaction was cautiously warmed to 60° C. as gas evolution can cause a froth to enter the balloon. The reaction mixture was stirred for 20 h at 65° C. It was diluted with dioxane and stirred for an additional 5 min. The warm solution was filtered through Celite, and the filtrate was concentrated in vacuo. Purification of the crude residue by flash column chromatography (silica gel, eluting with a gradient of ethyl acetate in hexanes) gave cyano-4-dimethylamino-2-ethoxy-benzoic acid methyl ester (218 mg, 12%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579368B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-03a8eac56e4f47a79667df6c73550674 |
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| Source note | uspto-grants-2009_08 |
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