HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930163Generated: October 31, 2026
Methyl iodide → 2-(3,5-Difluoro-4-methoxyphenyl)propanoic acid
https://huagongshe.com/reaction/1930163
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (3,5-Difluoro-4-methoxyphenyl)acetic acid | HCID 17750666 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3,5-Difluoro-4-methoxyphenyl)propanoic acid | HCID 59627718 | 105.1% |
Reaction Steps
Lithium bis(trimethylsilyl)amide (25.4 mL, 25.35 mmol) was added to 2-(3,5-difluoro-4-methoxyphenyl)acetic acid (2.5 g, 12.37 mmol) in THF (60.8 mL) cooled to 0° C. under nitrogen. The resulting solution was stirred at 0° C. for 30 minutes. Next Methyl iodide (0.925 mL, 14.84 mmol) was added and the reaction stirred for 30 minutes Ammonium chloride (satd) (50 mL) added with vigorous stirring, ethyl acetate (100 mL) and water (50 mL) were added and the organic phase separated, washed with water (50 mL) and saturated brine (50 mL). The aq layer was acidified with 2M HCl (50 mL) and extracted with ethyl acetate. The organic layers were combined and dried over MgSO4, filtered and evaporated to afford 2-(3,5-difluoro-4-methoxyphenyl)propanoic acid (2.81 g, 105%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188092B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-62892c92bbb945c5b38d69800f6c3067 |
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| Source note | uspto-grants-2012_05 |
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