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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558333Generated: October 29, 2026

Hydrochloric Acid → HCID 23141413, compound

https://huagongshe.com/reaction/558333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 23141460HCID 23141460—
SolventMethanolHCID 887—
ProductHCID 23141413HCID 23141413101.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Ethyl N-(4-trifluoromethoxyphenyl)-4-methoxy-isophthalamate (51 mg) obtained in step E was dissolved in 2 mL of methanol, and 0.8 mL of a 20% aqueous solution of potassium hydroxide was added. The resulting solution was stirred for 30 minutes at 80° C., and then cooled to room temperature. One M hydrochloric acid (3 mL) was used to adjust the solution to pH of about 3. Then, the resulting aqueous solution was extracted with ethyl acetate. The respective organic layers were combined, whereafter the combined organic layer was washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was separated by filtration, and washed with ethyl acetate. The filtrate and the washings were combined, and ethyl acetate was distilled off under reduced pressure to obtain 48 mg (100%) of N-(4-trifluoromethoxyphenyl)-4-methoxyisophthalamic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063046B2
Source datasetuspto-grants-2011_11
ORD IDord-f18bdecab7264292b6fb9b92b397bc3f
Source noteuspto-grants-2011_11