HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-(Dimethylamino)ethyl)triphenylphosphonium bromide → (E)-3-{6-[3-Dimethylamino-1-(4-tolyl)prop-1E-enyl]-2-pyridyl}acrylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-(Dimethylamino)ethyl)triphenylphosphonium bromide | HCID 2724136 | — |
| Reactant | (E)-3-[6-(p-toluoyl)-2-pyridyl]acrylic acid | HCID 11971260 | — |
| Product | (E)-3-{6-[3-Dimethylamino-1-(4-tolyl)prop-1E-enyl]-2-pyridyl}acrylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04657918 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-bb30646c33b748e8bfa63b5d63a33c6b |
| Source note | uspto-grants-1987_04 |