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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
Reactant5-Bromo-6-methoxypyridine-3-carbaldehydeHCID 12392416—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-bromo-2-methoxy-5-(2-methoxyvinyl)pyridineHCID 5820791485%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410128B2
Source datasetuspto-grants-2013_04
ORD IDord-ff82a8c028e34a3eb395f3bff4fe5835
Source noteuspto-grants-2013_04