HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488880Generated: October 30, 2026
Hydrochloric Acid → [7-Chloro-2-oxo-4-phenyl-6-[(4-phenylpiperazin-1-yl)methyl]-2h-chromen-3-yl]acetic acid
https://huagongshe.com/reaction/488880
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl [7-chloro-2-oxo-4-phenyl-6-[(4-phenylpiperazin-1-yl)methyl]-2h-chromen-3-yl]acetate.hydrochloride | HCID 131725236 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [7-Chloro-2-oxo-4-phenyl-6-[(4-phenylpiperazin-1-yl)methyl]-2h-chromen-3-yl]acetic acid | HCID 22267205 | 96.2% |
Reaction Steps
Ethyl [7-chloro-2-oxo-4-phenyl-6-[(4-phenylpiperazin-1-yl)methyl]-2H-chromen-3-yl]acetate.hydrochloride (40 g) was suspended in ethanol (120 ml), and combined with a 2 N aqueous solution of sodium hydroxide (144.5 ml). A yellow clear solution obtained by stirring at 70° C. for 1 hour was added dropwise to a mixture solution of ethanol (40 ml) and 6 N hydrochloric acid (49.4 ml) over 45 minutes. The reaction solution was adjusted to pH 5.5 to 6.0 with sodium hydrogen carbonate at 40° C. After pH became stable, the mixture was stirred at 35 to 40° C. internal temperature for 15 minutes, and cooled to room temperature, and stirred at room temperature for 30 minutes. The crystal formed was filtered and washed with 30% ethanol to obtain the title compound (34 g, yield: 96%) as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06974806B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-904ee024d0f248b78f0653a1e239daa3 |
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| Source note | uspto-grants-2005_12 |
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