Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Methyl 5-tert-butyl-1,2-oxazol-3-ylcarbamate | HCID 13309592 | — |
| Catalyst | Formic Acid | HCID 284 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22768144 | HCID 22768144 | 99.1% |
Reaction Steps
To a solution of methyl 5-t-butyl-3-isoxazolylcarbamate (2.00 g) and anhydrous sodium acetate (1.1 mol equivalent) in glacial acetic acid (5 ml), bromine (1.0 mol equivalent) is added. The resultant mixture is heated at 50° C for 53 hours and mixed with glacial acetic acid (5 ml), anhydrous sodium acetate (0.91 g) and bromine (0.81 g). The mixture is heated at 70° C for 31 hours, mixed with several drops of formic acid, poured onto ice water (50 ml) and shaken with methylene chloride. The organic layer is washed with a saturated aqueous solution of sodium bicarbonate and water in order and evaporated under reduced pressure to remove the solvent, whereby methyl 4-bromo-5-t-butyl-3-isoxazolylcarbamate (2.77 g) is obtained as an oil. I.R.: 1774, 1203 cm-1 (CCl4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04116671 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-3950083ac1324982b382b1d558455e08 |
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| Source note | uspto-grants-1978_09 |
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