HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12299Generated: October 29, 2026
Methyl iodide → Methyl 2-(4-chlorophenyl)-2-cyclopentylpropanoate
https://huagongshe.com/reaction/12299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Methyl 2-(4-chlorophenyl)-2-cyclopentylacetate | HCID 23092013 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Solvent | Butyllithium | HCID 178418339 | — |
| Product | Methyl 2-(4-chlorophenyl)-2-cyclopentylpropanoate | HCID 23092040 | — |
Reaction Steps
To a solution of diisopropylamine (0.15 ml) in THF (2 ml), n-butyl lithium (1.5 M hexane solution, 0.6 ml) was added at −78° C., stirred for 10 minutes and another solution of methyl 2-(4-chlorophenyl)-2-cyclopentylacetate (200 mg) in THF (1.5 ml) was added dropwise. After 15 minutes' stirring, the system temperature was raised to −35° C., and methyl iodide (0.15 ml) was added. The reaction liquid temperature was raised to 0° C., and the liquid was stirred for 1.5 hours, diluted with saturated aqueous ammonium chloride solution and extracted with diethyl ether. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and condensed under reduced pressure. The resulting residue was purified on silica gel column chromatography (hexane/ethyl acetate 60/1) to provide methyl 2-(4-chlorophenyl)-2-cyclopentylpropionate (180 mg) as yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727998B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-605b849843804862a90b8e36f41a45f4 |
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| Source note | uspto-grants-2010_06 |
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