HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357760Generated: November 1, 2026
Water → 3-Nitro-2-(phenylmethoxy)benzoic acid
https://huagongshe.com/reaction/2357760
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-Nitrosalicylic acid | HCID 6807 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Nitro-2-(phenylmethoxy)benzoic acid | HCID 22272669 | — |
Reaction Steps
To a solution of 2-hydroxy-3-nitrobenzoic acid (36.6 g) in N,N-dimethylformamide (500 mL) were added benzyl bromide (50.0 mL) and potassium carbonate (66.3 g), and the mixture was stirred overnight at 60° C. The reaction mixture was poured into water and the resulting mixture was extracted with a mixture of ethyl acetate and n-hexane (1:1). The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The residue was dissolved in a mixture of tetrahydrofuran (100 mL) and methanol (200 mL), and the resulting mixture was stirred for 30 minutes at 50° C. The reaction mixture was concentrated and the residue was acidified with 2N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated. The residue was recrystallized from isopropanol (50 mL)/n-hexane (200 mL) to give the title compound (31.99 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763610B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-c7dfdde8f48241e0b3e3453556ab0f4a |
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| Source note | uspto-grants-2010_07 |
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