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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodoacetate | HCID 5239 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | m-Chlorophenethylic alcohol | HCID 78856 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(3-Chloro-phenyl)-ethoxy]-acetic acid methyl ester | HCID 67098416 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928106B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-50c02981914a48769e8710de86a59d4b |
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| Source note | uspto-grants-2011_04 |
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