HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580950Generated: October 27, 2026
Allyl bromide → Ethyl 3-{4-[(prop-2-en-1-yl)oxy]phenyl}propanoate
https://huagongshe.com/reaction/580950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-hydroxyhydrocinnamate | HCID 2736435 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Ethyl 3-{4-[(prop-2-en-1-yl)oxy]phenyl}propanoate | HCID 19348971 | 97.2% |
Reaction Steps
Allyl bromide (2.30 g) was added to a stirred suspension of ethyl 3-(4-hydroxyphenyl)propionate (3.49 g) and anhydrous potassium carbonate (2.76 g) in butan-2-one (30 ml). The reaction mixture was heated at reflux for 18 hours. The reaction mixture was allowed to cool to ambient temperature and the mixture was filtered. The filtrate was evaporated to give an oil which was purified by column chromatography on silica gel (Merck.Art. No. 9385) using a 4:1 (v/v) mixture of n-hexane and ethyl acetate as eluent to give ethyl 3-(4-allyloxyphenyl)propionate (4.09 g) as a colourless oil; NMR (CDCl3): 1.22 (3H, t), 2.48 (2H, t), 2.88 (2H, t), 4.13 (2H, q), 4.51 (2H, m), 5.25-5.42 (2H, m), 5.95-6.15 (1H, m), 6.83 (2H, d) and 7.03 (2H, d); m/z 235 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05919793 |
|---|
| Source dataset | uspto-grants-1999_07 |
|---|
| ORD ID | ord-5a2bdee2237346168fe2f46f62cd61b0 |
|---|
| Source note | uspto-grants-1999_07 |
|---|