HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69405Generated: October 26, 2026
Methyl iodide → 4-Butoxy-2-methylbenzoic acid
https://huagongshe.com/reaction/69405
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 4-Butoxybenzoic acid | HCID 72971 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Butoxy-2-methylbenzoic acid | HCID 53439899 | — |
Reaction Steps
A mixture of 4-butoxybenzoic acid (10 g), N,N,N′,N′-tetramethylethylenediamine (13.2 g) and THF (75 mL) was cooled to −90° C., and sec-butyllithium (81 mL; 1.4 M in hexane) was added over the course of 30 minutes. After a further 30 minutes, the mixture was warmed to −78° C., and a solution of methyl iodide (12.8 mL) in THF (10 mL) was added dropwise. The reaction solution was allowed to warm to room temperature and the mixture was hydrolyzed with water and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated. The residue was purified by chromatography on silica gel. The product with the molecular weight of 208.26 (C12H16O3) was obtained in this way; MS (ESI): 209 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822495B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-9dbf2c0103ca4e578abbdbf1db5703e5 |
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| Source note | uspto-grants-2014_09 |
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