HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963213Generated: October 29, 2026
2-Bromophenol → Ethyl 4-(2-bromophenyloxy)but-2-enoate
https://huagongshe.com/reaction/963213
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl (E)-4-bromobut-2-enoate | HCID 5373944 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 4-(2-bromophenyloxy)but-2-enoate | HCID 54124865 | 74% |
Reaction Steps
To an acetone solution containing pulverized anhydrous K2CO3 (5.58 g, 40.5 mmol) and 2-bromophenol (5.0 g, 28.9 mmol) was added ethyl 4-bromocrotonate (6.69 g, 34.7 mmol). The mixture was stirred at 22° C. for 5 h and filtered. The filtrate was concentrated in vacuo and treated with 5% NaHCO3 (~10 mL). The residue and aqueous phase were extracted with CH2Cl2 (3×). The combined organic extracts were dried with anhydrous MgSO4, filtered, and concentrated in vacuo to afford the title compound (6.10 g, 74%) as a solid material which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763444 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-731d1aa040ab471d98045b57912f642c |
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| Source note | uspto-grants-1998_06 |
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