HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626773Generated: November 1, 2026
Hydrochloric Acid → {[4-(Adamantan-1-yl)phenyl]amino}(oxo)acetic acid
https://huagongshe.com/reaction/1626773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl {[4-(adamantan-1-yl)phenyl]amino}(oxo)acetate | HCID 66680869 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | {[4-(Adamantan-1-yl)phenyl]amino}(oxo)acetic acid | HCID 66679906 | 90% |
Reaction Steps
THF (18 mL) and ethanol (6 mL) were added to 600 mg (1.83 mmol) of ethyl {[4-(adamantan-1-yl)phenyl]amino}(oxo)acetate. Thereafter, 2.7 mL of 1N aqueous sodium hydroxide solution was added, and the mixture was heated at 70° C. for 2 hours. Next, 1N hydrochloric acid was added to acidify the mixture, and the organic solvent was distilled off under reduced pressure. The resulting solids were filtered and washed with H2O and n-hexane, followed by drying, thereby giving 492 mg of {[4-(adamantan-1-yl)phenyl]amino}(oxo)acetic acid (yield: 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785473B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-78912d8daaba418c96f03adb69966def |
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| Source note | uspto-grants-2014_07 |
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