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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542503Generated: October 25, 2026

(2-(Dimethylamino)ethyl)triphenylphosphonium bromide → (E)-3-{6-[3-Dimethylamino-1-(4-tolyl)prop-1E-enyl]-2-pyridyl}acrylic acid

https://huagongshe.com/reaction/542503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 2724136—
Reactant(E)-3-[6-(p-toluoyl)-2-pyridyl]acrylic acidHCID 11971260—
Product(E)-3-{6-[3-Dimethylamino-1-(4-tolyl)prop-1E-enyl]-2-pyridyl}acrylic acidHCID 13191753—

Reaction Steps

Treatment of (E)-3-[6-(4-toluoyl)-2-pyridyl]acrylic acid, vide supra, with the Wittig reagent derived from triphenyldimethylaminoethylphosphonium bromide by the method of example 1 gave a mixture of isomeric acids which were separated by fractional crystallization from ethyl acetate. The less-soluble E-isomer, (E)-3-{6-[3-dimethylamino-1-(4-tolyl)prop-1E-enyl]-2-pyridyl}acrylic acid was puried by crystallization from isopropanol, m.p. 222°-225° (decomp.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04657918
Source datasetuspto-grants-1987_04
ORD IDord-bb30646c33b748e8bfa63b5d63a33c6b
Source noteuspto-grants-1987_04