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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30340Generated: October 25, 2026

Water → 2-Amino-5-(4-methoxy-phenyl)-thiophene-3-carboxylic acid

https://huagongshe.com/reaction/30340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-5-(4-methoxy-phenyl)-thiophene-3-carboxylic acid methyl esterHCID 68963567—
SolventMethanolHCID 887—
Product2-Amino-5-(4-methoxy-phenyl)-thiophene-3-carboxylic acidHCID 6895797591%

Reaction Steps

To a stirred solution of 2-amino-5-(4-methoxy-phenyl)-thiophene-3-carboxylic acid methyl ester (6.6 g, 26.6 mmol) in MeOH (200 mL) was added 6N NaOH (100 mL) and water (50 mL). The reaction was heated to reflux for 2 h or until starting material was gone by TLC or LCMS. The solution was concentrated under vacuum to about half of the original volume. The pH of the resultant cloudy mixture was adjusted to 3-5 by the careful addition of 6N HCl (˜150 mL) while stirring. The gummy red precipitate was filtered and dried. Purification was achieved by triturating in boiling hexanes. The product (6.0 g, 91%) was isolated in pure form by filtration after cooling to room temperature and drying in a vacuum oven overnight. 1H NMR (d6-DMSO δ 7.37, d, 2H, δ 7.11, s, 1H; δ 7.10, br s, 2H; δ 6.94, d, 2H), LC/MS (APCI, ES, M+H=250).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423061B2
Source datasetuspto-grants-2008_09
ORD IDord-53951d626cc64e1db4cdb53e1bcc500e
Source noteuspto-grants-2008_09