HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851660Generated: October 30, 2026
Hydrochloric Acid → HCID 20500796, compound
https://huagongshe.com/reaction/851660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-(Trifluoromethyl)benzoyl fluoride | HCID 67606 | — |
| Reactant | 8-(4-Methoxyphenylamino)-caprylic acid | HCID 13025815 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20500796 | HCID 20500796 | — |
Reaction Steps
6.1 g (23 mmol) of 8-(4-Methoxyphenylamino)-caprylic acid are dissolved in 40 cc. of 0.2 n soda lye. A solution of 4.4 g (23 mmol) of 3-(Trifluoromethyl)-benzoic acid fluoride in 50 cc. of ether are added thereto within 20 minutes with vivid stirring dropwise at 25° C., holding the pH at between 7.2 and 8 by the dropwise addition of 0.2 n soda lye. After the addition, vivid stirring is continued for 30 minutes. The mixture is then acidified to pH 3 by the addition of 2 n hydrochloric acid. The aqueous and ethereal layers are separated. The aqueous phase is extracted several times with ether and then is rendered alkaline by the addition of calcium hydroxide. The separated calcium fluoride is filtered off with suction and is discarded. The purified ethereal phase is shaken with water, dried over MgSO4 and the solvent is distilled off. The residue is purified chromatographically on silicic acid gel using chloroform as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04386031 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-ee0feb31a7cd4d58a8e68e143d13769a |
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| Source note | uspto-grants-1983_05 |
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