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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298168Generated: October 31, 2026

Iodoethane → Ethyl 3-(bromophenyl)acetate

https://huagongshe.com/reaction/2298168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Bromophenyl)acetic acidHCID 74653—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-(bromophenyl)acetateHCID 1147055282.3%

Reaction Steps

To a solution of 3-bromophenylacetic Acid (10.0 g, 46.5 mmol) in CH3CN (150 mL) was added K2CO3 (7.39 g, 53.5 mmol) followed by ethyl iodide (5.6 mL, 70.0 mmol). The mixture was heated at reflux for 2.5 h and was cooled to room temperature. The volatiles were removed in vacuo and water was added. The aqueous solution was extracted with EtOAc (3×) and the combined organic extracts were washed with brine. The organic solution was dried (MgSO4), filtered, and concentrated to provide (3-bromo-phenyl)-acetic Acid ethyl ester (9.30 g) as an oil. 1H NMR (400 MHz, CDCl3) δ 7.43 (s, 1H), 7.38 (m, 1H), 7.21-7.16 (m, 2H), 4.14 (q, 2H), 3.56 (s, 2H), 1.24 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492412B2
Source datasetuspto-grants-2002_12
ORD IDord-f8b7ead7473442b79a394f91f3c2f6fb
Source noteuspto-grants-2002_12