Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 57912472 | HCID 57912472 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 57912479 | HCID 57912479 | 46% |
Reaction Steps
Prepared according to general procedure A using tert-butyl 3-(2-hydroxy4-methoxyphenyl)-3-oxopropanoate (532 mg, 2.0 mmol), benzaldehyde (200 μL, 2.00 mmol), 12.0 mL benzene, piperidine (10 μL, 0.10 mmol) and glacial acetic acid (5.7 μL, 0.10 mmol), refluxed for 3 h. Purified via recrystallization from hexanes/CH2Cl2, yielding 321 mg (46%) of white solid. mp=105-107° C.; IR (film) 2977.5; 1712.8; 1624.0; 1155.6 cm−1; 1H NMR (500 MHz, CDCl3) δ 12.41 (bs, 1H), 7.81 (s, 1H), 7.41 (d, J=9.1 Hz, 1H), 7.37-7.25 (m, 5H), 6.46 (d, J=2.1 Hz, 1H), 6.34 (dd, J=8.8, 2.1 Hz, 1H), 3.83 (s, 3H), 1.42 (s, 9H); 13C NMR (125 MHz, CDCl3) δ 199.4, 166.8, 165.8, 164.0, 141.8, 133.6, 133.1, 131.6, 130.5, 130.3, 129.1, 114.3, 108.4, 101.1, 82.6, 55.8, 28.1; LRMS (electrospray): Mass calculated for C21H22O5 [M]+, 354.14. Found [M+23]+, 377.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851640B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-984f96aa540e4ff8a6cc34c341a50b3f |
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| Source note | uspto-grants-2010_12 |
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