HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128902Generated: October 29, 2026
Methyl Salicylate → HCID 22904479, compound
https://huagongshe.com/reaction/128902
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Salicylate | HCID 4133 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22904479 | HCID 22904479 | — |
Reaction Steps
Dimethylformamide (DMF)(100 ml), potassium carbonate (17.97 g) and 2,4-dichlorobenzyl chloride (21.50 g) were added to methyl salicylate (15.22 g), and the mixture was stirred at room temperature overnight. Ethyl acetate (1000 ml) was added to the reaction mixture, and the resulting mixture was washed with brine (700 ml) twice, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give crude methyl 2-(2,4-dichlorobenzyloxy)benzoate. Methanol (100 ml), THF (100 ml), water (20 ml) and 85% potassium hydroxide (7.92 g) were added to the crude product thus obtained, and the mixture was stirred at 60° C. for 2 hours. After completion of the reaction, the mixture was concentrated under reduced pressure. Water (300 ml) was added to the residue, and the pH of the mixture was adjusted to not more than 2, and the resulting crystals were separated by filtration, dried to give 2-(2,4-dichlorobenzyloxy)benzoic acid (29.30 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05466661 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-70c3c1d2eb794ec1a2ce8296bca0f4ec |
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| Source note | uspto-grants-1995_11 |
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