HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872402Generated: October 26, 2026
Triethylamine → Methyl 4-(5-(4-(pentyloxy)phenyl)isoxazol-3-yl)benzoate
https://huagongshe.com/reaction/1872402
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Eth-1-ynyl-4-(pentyloxy)benzene | HCID 2775119 | — |
| Reactant | alpha-Chloro-4-methoxycarbonylbenzaldoxime | HCID 73989494 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(5-(4-(pentyloxy)phenyl)isoxazol-3-yl)benzoate | HCID 10737571 | 84.6% |
Reaction Steps
To a solution of 4-Methoxycarbonylphenylhydroxyiminomethyl chloride (16.98 g) and 4-n-pentyloxyphenylacetylene (18.96 g) in tetrahydrofuran (170 ml) was added triethylamine (14.4 ml) in tetrahydrofuran (140 ml) over a period of 2 hours at 40° C. and the mixture was stirred at 40° C. for 30 minutes. The mixture was diluted with dichloromethane and washed with water and brine. The separated organic layer was dried over magnesium sulfate and evaporated under reduced pressure. The residue was triturated with acetonitrile. The precipitate was collected by filtration and dried to give Methyl 4-[5-(4-n-pentyloxyphenyl)isoxazol-3-yl]benzoate (24.56 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06107458 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-b78335e158dd48b8bd5da9f7ec3aed03 |
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| Source note | uspto-grants-2000_08 |
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