HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488601Generated: October 30, 2026
Methyl iodide → 3-(4-Chlorophenyl)-2-methylpropanoic acid
https://huagongshe.com/reaction/488601
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | beta-(p-Chlorophenyl)propionic acid | HCID 123137 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Chlorophenyl)-2-methylpropanoic acid | HCID 22270652 | — |
Reaction Steps
A solution of 3-(4-chlorophenyl)propionic acid (1.85 g, 10 mmol) in 10 mL THF was added to 16 mL freshly prepared 1.5 M LDA (24 mmol) at dryice-acetone bath temp. The reaction mixture was stirred 1 hr as it warmed to −30° C. and 1.6 mL (25 mmol) of methyl iodide was added. The resulting mixture was stirred at the same temp. for 0.5 h and the stirring was continued at RT overnight. The reaction was quenched with 1 N HCl, and diluted with ether. The solution was washed with water, 10% sodium thiosulfate and brine. The organic layer was dried over MgSO4. Solvent removal gave a mixture of the desired methylated product and the starting acid. Repetition of the above procedure on this residue gave 1.3 g the desired 2-methyl-3-(4-chlorophenyl) propionic acid contaminated with ˜5% of the starting acid as an oil. NMR: 1.5 (d, 3H), 4.78 (q, 1H). 6.84 & 7.26 (2d, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06972295B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-c672f252463d4d26bea035a02dcf94e6 |
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| Source note | uspto-grants-2005_12 |
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