HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → methyl(2E)-3-[4-(3-bromopropoxy)phenyl]prop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl p-coumarate | HCID 92203 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | Bromopropanol | HCID 12887879 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl(2E)-3-[4-(3-bromopropoxy)phenyl]prop-2-enoate | HCID 70495691 | — |
Reaction Steps
To a solution 5 g (28.1 mmol) of 4-Hydroxycinnamic acid methyl ester, 4.9 g (35.1 mmol) of 4 bromopropanol, 9.2 g (35.1 mmol) of triphenylphosphine in 100 mL of THF are added 7.1 g (35.1 mmol) of diisopropylazodicarboxylate under inert atmosphere. The solution is heated up to reflux and allowed to stir overnight. After 20 hours, the reaction mixture is partitioned between EtOAc and water. The organic phase is washed repeatedly with water, dried over sodium sulphate, filtered and concentrated by rotary evaporation to give 7.5 g of (methyl (2E)-3-[4-(3-bromopropoxy)phenyl]prop-2-enoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09334366B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-db9adabeb650425a934951281dbbebef |
| Source note | uspto-grants-2016_05 |