HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558333Generated: October 29, 2026
Hydrochloric Acid → HCID 23141413, compound
https://huagongshe.com/reaction/558333
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 23141460 | HCID 23141460 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23141413 | HCID 23141413 | 101.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063046B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-f18bdecab7264292b6fb9b92b397bc3f |
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| Source note | uspto-grants-2011_11 |
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