Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Putrescine | HCID 1045 | — |
| Reactant | 4-Chloro-3,5-dimethylisoxazole | HCID 539493 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21451296 | HCID 21451296 | — |
Reaction Steps
A mixture of 12 g of 4-chloro-3,5-dimethyl isoxazole (prepared by chlorination of 3,5-dimethyl-isoxazole in acetic acid at 50° C) in freshly distilled THF and 13.8 ml of tetramethylenediamine in a 3-necked vessel was reacted under a nitrogen atmosphere with 50 ml of a 20% n-butyl lithium solution in hexane at -70° C and the mixture was stirred for 2 hours. A stream of carbon dioxide was passed therethrough for an hour and then water and diethyl ether were added thereto. The aqueous layer was extracted with diethyl ether at a pH of 2 and the combined organic layers were dried over magnesium sulfate, treated with activated carbon and concentrated to dryness under reduced pressure. The 6.3 g of product was crystallized from a petroleum ether-acetone mixture to obtain 3-methyl-4-chloro-isoxazole-5-yl acetic acid melting at 128°-131° C (sublimation)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04010264 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-13c3bb98ad634f0782ebc959e1d835f6 |
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| Source note | uspto-grants-1977_03 |
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