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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595862Generated: November 2, 2026

Iodoethane → Ethyl 3-(bromophenyl)acetate

https://huagongshe.com/reaction/1595862

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 numberUS06288120B1
Source datasetuspto-grants-2001_09
ORD IDord-4f20208e76dd43e38f005b6b6f0ce6b7
Source noteuspto-grants-2001_09