Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 66932609 | HCID 66932609 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66932439 | HCID 66932439 | 105.5% |
Reaction Steps
(E)-3-{1′-(2-Phenyl-ethyl)-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid methyl ester (1.70 g, 4.19 mmol) was dissolved in acetic acid (20 ml). 6 M HCl (20 ml) was added and the resulting suspension was heated at 85° C. for 4 h, then the solvents were evaporated and the residue was dried under vacuum, giving (E)-3-{1′-(2-phenyl-ethyl)-4-oxo-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid (1.73 g) as a light yellow solid (hydrochloride salt).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592444B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-ba710920a73e49baa0f53cc7a149e013 |
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| Source note | uspto-grants-2013_11 |
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