Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Hydroxyphenyl)-terephthalamic acid methyl ester | HCID 68619610 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-(benzoxazol-2-yl)benzoate | HCID 650931 | 91.1% |
Reaction Steps
A solution of (2-hydroxyphenyl)-terephthalamic acid methyl ester (0.35 g, 1.3 mmol) in polyphosphoric acid (5 mL) was heated to reflux for 3 h. The solution was cooled to 0° C., water added (100 mL) and solid K2CO3 introduced until pH 7-9 was attained. The residue was diluted with ethyl acetate (2×100 mL) and the organic extract dried (MgSO4), filtered and concentrated to give cyclized methyl 4-(benzoxazol-2-yl)-benzoate (0.15 g, 45%) as a beige powder. 1H NMR (CDCl3) δ3.98 (s, 3H), 7.40 (m, 2H), 7.61 (m, 1H), 7.81 (m, 1H), 8.20 (d, 2H, J=7.8 Hz), 8.34 (d, 2H, J=7.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06734191B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-bea50f8c962742cea2d44bad72a56cce |
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| Source note | uspto-grants-2004_05 |
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