HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927721Generated: October 28, 2026
Methylparaben → Methyl 4-(4-(2-tert-butoxy-2-oxoethyl)-2-cyanophenoxy)benzoate
https://huagongshe.com/reaction/1927721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylparaben | HCID 7456 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tert-butyl 2-(3-cyano-4-fluorophenyl)acetate | HCID 45925946 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | Methyl 4-(4-(2-tert-butoxy-2-oxoethyl)-2-cyanophenoxy)benzoate | HCID 68466372 | 65.3% |
Reaction Steps
tert-Butyl 2-(3-cyano-4-fluorophenyl)acetate (2.6 g, 11.1 mmol) and methyl 4-hydroxybenzoate (3.36 g, 22.1 mmol) were diluted with DMSO (22 mL) followed by the addition of potassium carbonate (1.83 g, 13.3 mmol). The reaction mixture was heated to 125° C. and stirred for 5 hours. The reaction mixture was diluted with ethyl acetate and 10% aqueous sodium carbonate. The layers were separated and the organic layer was washed with 10% aqueous sodium carbonate two more times followed by water and brine. The organic material was dried over MgSO4, filtered and concentrated. The material was purified using a biotage 40M column eluting with hexanes:ethyl acetate (9:1) to yield methyl 4-(4-(2-tert-butoxy-2-oxoethyl)-2-cyanophenoxy)benzoate (2.65 g, 65.3% yield) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183289B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-5681aace3c8c4f9990e783c66cb9cc32 |
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| Source note | uspto-grants-2012_05 |
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