HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375655Generated: October 31, 2026
Triethylamine → 5-(3-(3-Oxo-butyl)-phenyl)-isoxazole-3-carboxylic Acid Methyl Ester
https://huagongshe.com/reaction/1375655
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Buten-2-ol | HCID 11716 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Methyl 5-(3-bromophenyl)isoxazole-3-carboxylate | HCID 53393795 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(3-(3-Oxo-butyl)-phenyl)-isoxazole-3-carboxylic Acid Methyl Ester | HCID 69508096 | 59.4% |
Reaction Steps
To a mixture of 5-(3-Bromo-phenyl)-isoxazole-3-carboxylic acid methyl ester (1.5 g, 5.3 mmol), Pd(OAc)2 (60 mg, 0.27 mmol), P(o-tolyl)3 (162 mg, 0.53 mmol) in anhydrous N,N-dimethylformamide (15 mL) in a pressure tube was added 3-buten-2-ol (0.92 mL, 10.6 mmol) and triethylamine (1.1 mL, 7.95 mmol). The mixture was flushed with nitrogen for 3 minutes, capped and heated to 100° C. for 30 minutes. The reaction mixture was allowed to cool to ambient temperature, partitioned between ethyl acetate and water (75 mL, 1:1). The organic layer was washed with brine (2×25 mL), dried (Na2SO4), filtered, concentrated under reduced pressure and purified on a Silica Gel MPLC eluting with 20–40% ethyl acetate/hexanes to provide the titled compound as a light yellow solid (860 mg, 59%). MS (ESI(+)) m/e 274 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169797B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-93c2b8de9d8549a5bef97182f8516e1d |
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| Source note | uspto-grants-2007_01 |
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