HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365047Generated: October 30, 2026
Methyl 4-Formylbenzoate → 4-(Phenyl-1-butenyl)benzoic acid, methyl ester
https://huagongshe.com/reaction/365047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-Formylbenzoate | HCID 15294 | — |
| Reactant | 3-Phenylpropyl triphenylphosphonium bromide | HCID 10928647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Phenyl-1-butenyl)benzoic acid, methyl ester | HCID 54000744 | — |
Reaction Steps
To a 0° solution of phenylpropyl triphenylphosphonium bromide (3.55 g, 1.25 eq) in 30 ml of dry THF under argon was added K-t-amylate (3.9 ml, 1.1 eq). After stirring for 30 minutes at 0° C. then allowing to warm to room temperature, a solution of 4-formylbenzoic acid methyl ester (1.0 g, 6.1 mmol) in ~8 ml of dry THF was added dropwise. This solution was stirred for 3 hours at room temperature, then diluted with ~1 ml of H2O, and concentrated to remove most of the THF. EtOAc (~200 ml) was added and the mixture was washed with H2O, 1N HCl (2×) and brine. After drying over anhydrous MgSO4, the solvent was removed in vacuo to yield a yellow oil which solidified soon after. Column purification of this crude product was done on a 50 mm column on silica gel eluted with 95:5 hexane/EtOAc. Product containing fractions were combined to yield after concentration title compound, 1.5 g (93%) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04607053 |
|---|
| Source dataset | uspto-grants-1986_08 |
|---|
| ORD ID | ord-e7eb046364194948818c9999a268ad93 |
|---|
| Source note | uspto-grants-1986_08 |
|---|