HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051865Generated: October 27, 2026
Methyl iodide → Methyl 4-fluoro-alpha-methylbenzeneacetate
https://huagongshe.com/reaction/1051865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Methyl 2-(4-fluorophenyl)acetate | HCID 2733233 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Methyl 4-fluoro-alpha-methylbenzeneacetate | HCID 11389760 | 96.9% |
Reaction Steps
To a stirred solution of diisopropylamine (13.0 g) in tetrahydrofurane (160 mL) was added a solution of n-butyllithium in hexane (51.4 mL; c=2.5 M) at −78° C. The solution was stirred at 0° C. for 15 minutes. The solution was cooled to −78° C. and a solution of methyl (4-fluorophenyl)acetate (18.0 g), dissolved in tetrahydrofurane (40 mL) was added. The solution was stirred at −78° C. for 30 minutes. Methyl iodide (10.0 mL) was added at −78° C., and the solution was allowed to warm up to 0° C. within 1 h. Water was added and the reaction mixture was extracted with ethyl acetate. The organic phase was dried (sodium sulfate) and the solvent was removed in vacuum. Silicagel chromatography gave 18.9 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388177B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-e2ac11216b984749951074ec26cb127c |
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| Source note | uspto-grants-2016_07 |
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