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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076821Generated: October 27, 2026

Sodium Iodoacetate → [2-(3-Chloro-phenyl)-ethoxy]-acetic acid methyl ester

https://huagongshe.com/reaction/2076821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodoacetateHCID 5239—
ReactantThionyl ChlorideHCID 24386—
Reactantm-Chlorophenethylic alcoholHCID 78856—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product[2-(3-Chloro-phenyl)-ethoxy]-acetic acid methyl esterHCID 6709841676%

Reaction Steps

To a solution of 2-(3-chloro-phenyl)-ethanol (1.96 g, 12.51 mmol) in THF (55 ml) was added n-BuLi (8.8 ml, 1.6 M solution in hexane, 13.77 mmol) at −78° C. Then sodium iodoacetate (2.6 g, 12.51 mmol) was added and the mixture was allowed to warm to ambient temperature and was stirred overnight. The THF was then removed and 1 N HCl was added to the remaining residue to adjust the pH to 1. This mixture was extracted two times with dichloromethane and the combined extracts were dried (Na2SO4) and evaporated. The remaining red liquid was dissolved in MeOH (60 ml) and thionylchloride (1.56 ml, 21.5 mmol) was added dropwise at −15° C. The reaction mixture was then stirred for 1.5 h at ambient temperature. Then water was added and the mixture was extracted three times with ether. The combined extracts were washed with brine, dried (Na2SO4) and evaporated. The remaining residue was then purified by column chromatography (silica gel, heptane/ethyl acetate 95:5 to 88:12) to give the title compound (2.161 g, 9.45 mmol; 76%) as orange liquid. MS: m/e=229.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928106B2
Source datasetuspto-grants-2011_04
ORD IDord-50c02981914a48769e8710de86a59d4b
Source noteuspto-grants-2011_04