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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl (E)-4-bromobut-2-enoateHCID 5373944—
SolventAcetoneHCID 180—
ProductEthyl 4-(2-bromophenyloxy)but-2-enoateHCID 5412486574%

Reaction Conditions

Temperature22 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763444
Source datasetuspto-grants-1998_06
ORD IDord-731d1aa040ab471d98045b57912f642c
Source noteuspto-grants-1998_06