HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454618Generated: October 30, 2026
Hydrochloric Acid → HCID 58508776, compound
https://huagongshe.com/reaction/454618
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 58508925 | HCID 58508925 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58508776 | HCID 58508776 | 45.8% |
Reaction Steps
Dioxane (1.0 mL) and 6 mol/L hydrochloric acid (1.0 mL) were added to the obtained tert-butyl 2-(5-(1,4-dioxa-8-azaspiro[4,5]decan-8-yl)-2-hydroxybenzamido)-4-phenylbenzoate (0.070 g), followed by heating to reflux for 25 minutes. The reaction mixture was cooled to room temperature, and water and ethyl acetate were added thereto, followed by adjusting the pH to 5.2 with a saturated aqueous solution of sodium bicarbonate. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Kanto Chemical Co., Inc., silica gel 60 (spherical), eluent: chloroform] to obtain 0.026 g of 2-(2-hydroxy-5-(4-oxopiperidin-1-yl)benzamido)-4-phenylbenzoic acid as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492582B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-fd77414e8af6479eb9165076f36da269 |
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| Source note | uspto-grants-2013_07 |
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