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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183665Generated: October 26, 2026

Sodium Hydroxide → 2-(3-(Cyclopropylmethoxy)-4-nitrophenyl)acetic acid

https://huagongshe.com/reaction/1183665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantDiethyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)malonateHCID 57995590—
SolventEthanolHCID 702—
Product2-(3-(Cyclopropylmethoxy)-4-nitrophenyl)acetic acidHCID 5799554090.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Compound diethyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)malonate (10 g) was dissolved in 100 mL ethanol and cooled to 0° C., NaOH solution (4 eq) was added slowly to the reaction mixture for about 15 min. The reaction mixture was heated gently up to 60° C. for 5 h. Progress of the reaction was monitored by TLC analysis. After complete conversion of starting material solvent was evaporated under reduced pressure, residue dissolved in H2O, acidified with 6N HCl to pH-2. Filtered the solid material washed with water, dried under reduced pressure to give 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)acetic acid (6.5 g) as a yellow solid. 1H-NMR (CDCl3, 200 MHz): 0.36 (m, 2H), 0.58 (m, 2H), 1.28 (m, 1H), 3.71 (s, 2H), 4.01 (d, 2H), 7.02 (d, 1H), 7.23 (s, 1H), 7.81 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664249B2
Source datasetuspto-grants-2014_03
ORD IDord-cfa1ad7be7f24ff2b36091719152dfe6
Source noteuspto-grants-2014_03