HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095009Generated: October 30, 2026
5-Hydroxy-2-nitrobenzoic acid → Methyl 5-hydroxy-2-nitrobenzoate
https://huagongshe.com/reaction/1095009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Hydroxy-2-nitrobenzoic acid | HCID 11882 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 2-amino-4,5-bis(2-methoxyethoxy)benzoate | HCID 11347513 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-hydroxy-2-nitrobenzoate | HCID 12922678 | — |
Reaction Steps
5-Hydroxy-2-nitro-benzoic acid (compound A′) (2.0 g) was dissolved in methanol (30 ml). Thionyl chloride (3.0 ml) was added dropwise to the solution on an ice bath, and the mixture was then stirred at 75° C. for 96 hr. After the completion of the reaction, the reaction solution was neutralized with a saturated aqueous sodium hydrogencarbonate solution and was then subjected to separatory extraction with ethyl acetate. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated under the reduced pressure to give crude 5-hydroxy-2-nitro-benzoic acid methyl ester (2.2 g, crude yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134015B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-db9efb25a24c4dda9927ce199ee8c24e |
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| Source note | uspto-grants-2012_03 |
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