HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958468Generated: November 1, 2026
Methoxymethyl-triphenylphosphonium chloride → (E)-3-bromo-2-methoxy-5-(2-methoxyvinyl)pyridine
https://huagongshe.com/reaction/1958468
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | 5-Bromo-6-methoxypyridine-3-carbaldehyde | HCID 12392416 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-3-bromo-2-methoxy-5-(2-methoxyvinyl)pyridine | HCID 58207914 | 85% |
Reaction Steps
A solution of (methoxymethyl)triphenylphosphonium chloride (737 mg, 2.15 mmol) in THF (10 mL) at −78° C. was added t-BuOK (1 M in THF, 2.15 mL, 2.15 mmol) and stirred at 0° C. for 30 mins, then added dropwisely a solution of 5-bromo-6-methoxynicotinaldehyde (310 mg, 1.435 mmol) in THF (6 mL) at 0° C. via cannulation. The mixture was stirred and gradually warmed to rt overnight. The mixture was concentrated and the residue was purified via a flash column using 50% ethyl acetate in hexanes as an eluent. The product containing fractions were concentrated to give (E)-3-bromo-2-methoxy-5-(2-methoxyvinyl)pyridine (296.9 mg, 85% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410128B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-ff82a8c028e34a3eb395f3bff4fe5835 |
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| Source note | uspto-grants-2013_04 |
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