HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637885Generated: October 25, 2026
(2-(Dimethylamino)ethyl)triphenylphosphonium bromide → (E)-3-[4-(3-Dimethylaminopropenyl)phenyl]acrylic Acid
https://huagongshe.com/reaction/1637885
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2-(Dimethylamino)ethyl)triphenylphosphonium bromide | HCID 2724136 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | Methyl 3-(4-formylphenyl)-2-propenoate | HCID 53401287 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-3-[4-(3-Dimethylaminopropenyl)phenyl]acrylic Acid | HCID 70098974 | 34% |
| Product | (E)-3-[4-(3-dimethylaminopropenyl)phenyl]acrylic acid, methyl ester | HCID 86755260 | — |
Reaction Steps
(E)-3-[4-(3-Dimethylaminopropenyl)phenyl]acrylic acid, methyl ester was prepared by the following way: (2-dimethylaminoethyl)triphenylphosphonium bromide (7.2 g, 17.4 mmol) in 30 mL of DMF was treated with KHMDS (27 mL, 1.01 equiv., 0.5 M in toluene) at -78° C. for one hour. At -40° C., 3-(4-formylphenyl)acrylic acid, methyl ester (2.54 g, 13.3 mmol, prepared according to the procedure of Syper et al., Synthesis, 1984, 9, 747-752) was added dropwise. The resulting mixture was stirred for 12 hours at rt and quenched with water. Extraction with EtOAc, drying over MgSO4 and evaporation in vacuo gave a residue that was purified via flash chromatography with DCM:MeOH (90:10) as eluting solvent. The title compound (1.1 g, 34%) was obtained as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06043252 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-87718733d0ef42998d8014a62451a771 |
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| Source note | uspto-grants-2000_03 |
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