HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374284Generated: October 30, 2026
Potassium Carbonate → 5-(4-Methoxy-2,5-dimethylphenoxy)-2,2-dimethyl-pentanoic acid, methyl ester
https://huagongshe.com/reaction/374284
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-bromo-2,2-dimethylpentanoate | HCID 13050502 | — |
| Reactant | 4-Methoxy-2,5-dimethylphenol | HCID 13751140 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(4-Methoxy-2,5-dimethylphenoxy)-2,2-dimethyl-pentanoic acid, methyl ester | HCID 86746385 | — |
Reaction Steps
A 500 mL, 3 neck round bottom flask is charged with 7.6 g (50 mmol) of 4-methoxy-2,5-xylenol, 8.3 g (60 mmol) of anhydrous potassium carbonate 13.4 g (60 mmol) of 5-bromo-2,2-dimethylvaleric acid, methyl ester (U.S. Pat. No. 4,665,226) and 150 mL of acetonitrile. The mixture is stirred mechanically at reflux for 24 hours. The reaction flask and inorganic solids are washed with fresh acetonitrile and the filtrate evaporated. The residue is taken up in diethyl ether and the solution washed with 50 mL of 2N potassium hydroxide solution, brine, dried (magnesium sulfate) and evaporated. The crude product amounts to 16.6 g. Distillation through a short path apparatus first at aspirator pressure and then at 0.5 mm affords 12.9 g of the title compound; infrared spectrum (IR) (C=0) 1732 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166398 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-caf57d8f8dd14906a03aa79932c753d1 |
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| Source note | uspto-grants-1992_11 |
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