HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → methyl 3(E)-[4-ethoxy-3-propoxyphenyl]acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22987074 | HCID 22987074 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | methyl 3(E)-[4-ethoxy-3-propoxyphenyl]acrylate | HCID 22987083 | — |
Reaction Steps
0.49 ml (6.60 mmol) of ethyl bromide and 1.37 g (9.9 mmol) of potassium carbonate are added to a mixture of 780 mg (3.30 mmol) of methyl (E)-4-hydroxy-3-propoxycinnamate and 10 ml of 2-butanone and then refluxed for 2 hours. Thereafter, the reaction mixture is cooled to room temperature and is partitioned between ethyl acetate and water, and the organic phase is washed several times with water, dried over magnesium sulfate, filtered and evaporated down. Chromatography of the residue over silica gel using 9:1 cyclohexane/ethyl acetate gives methyl 3(E)-[4-ethoxy-3-propoxyphenyl]acrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06632909B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-719c79daf1a94cbebeadbab72621b48e |
| Source note | uspto-grants-2003_10 |