HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217292Generated: October 27, 2026
Sodium Hydroxide → 2-(Carboxymethyl)-4-nitrobenzoic acid
https://huagongshe.com/reaction/217292
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(1,3-Dimethoxy-1,3-dioxopropan-2-yl)-4-nitrobenzoic acid | HCID 10590078 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Carboxymethyl)-4-nitrobenzoic acid | HCID 7172025 | 23.3% |
Reaction Steps
A solution of sodium hydroxide (5.0 g, 125 mmol) in water (60 mL) was added to a solution of dimethyl 2-(2-carboxy-5-nitrophenyl)malonate (7.0 g, 21.5 mmol) in methanol (60 mL) at room temperature. After the reaction solution was stirred at room temperature for 3 hours, methanol was distilled off. The resulting residue was acidified using 1N hydrochloric acid (11 mL). The suspension was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a crude product. After the crude product was stirred in ethyl acetate (20 mL) at 70 to 80° C. overnight, the temperature was allowed to return to room temperature. The precipitate was collected by filtration, and dried under reduced pressure to give the title compound (1.13 g, 23%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08193351B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-df486528467a40439168e9efa63e6064 |
|---|
| Source note | uspto-grants-2012_06 |
|---|