HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845692Generated: October 27, 2026
Potassium Carbonate → 2-(4-benzyloxyphenoxy)propionic acid N-cyano-N-methylamide
https://huagongshe.com/reaction/845692
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromopropionic acid N-cyano-N-methylamide | HCID 53744792 | — |
| Reactant | 2-[2-[[2-(2,5-Dihydroxyphenyl)phenyl]methoxymethyl]phenyl]benzene-1,4-diol | HCID 131711022 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-benzyloxyphenoxy)propionic acid N-cyano-N-methylamide | HCID 54526351 | 63% |
Reaction Steps
With efficient stirring, B 19.1 g (0.1 mole) of 2-bromopropionic acid N-cyano-N-methylamide are added dropwise to a solution of 20.0 g (0.1 mole) of hydroquinone monobenzyl ether and 16.5 g (0.12 mole) of potassium carbonate in 200 ml of dimethylformamide. After the slightly exothermic reaction has subsided, the reaction mixture is heated for 3 hours to 40° C. The precipitated salts are then removed by filtration and the filtrate is concentrated by evaporation. The residue is dissolved in ether and the ether solution is extracted with dilute sodium hydroxide solution. The organic phase is dried over sodium sulfate, the solvent is evaporated off and the residue is distilled in vacuo, affording 19.5 g (63% of theory) of 2-(4-benzyloxyphenoxy)propionic acid N-cyano-N-methylamide with a melting point of 56°-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04759796 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-b8a4e543e28e4193a37b5632288dddc1 |
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| Source note | uspto-grants-1988_07 |
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