HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553734Generated: October 31, 2026
Hydroxyamine hydrochloride → Methyl 5-(4-bromo-2-chlorophenyl)-3-methyl-4-isoxazolecarboxylate
https://huagongshe.com/reaction/553734
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 178483596 | HCID 178483596 | — |
| Product | Methyl 5-(4-bromo-2-chlorophenyl)-3-methyl-4-isoxazolecarboxylate | HCID 58539615 | — |
Reaction Steps
Following the procedures described in Example 36: 4-bromo-2-chlorobenzoic acid and oxalyl chloride were reacted to provide 4-bromo-2-chloro-benzoyl chloride, which was reacted with 3-methylamino-but-2-enoic acid methyl ester to provide 2-(4-bromo-2-chloro-benzoyl)-3-[(E)-methylimino]-butyric acid methyl ester. 2-(4-Bromo-2-chloro-benzoyl)-3-[(E)-methylimino]-butyric acid methyl ester and hydroxylamine hydrochloride were then reacted to provide 5-(4-bromo-2-chloro-phenyl)-3-methyl-isoxazole-4-carboxylic acid methyl ester. Following Example 36, Step 4, 5-(4-bromo-2-chloro-phenyl)-3-methyl-isoxazole-4-carboxylic acid methyl ester was hydrolyzed to 5-(4-bromo-2-chloro-phenyl)-3-methyl-isoxazole-4-carboxylic acid. 5-(4-Bromo-2-chloro-phenyl)-3-methyl-isoxazole-4-carboxylic acid and (R)-1-(2-chloro-phenyl)-ethanol were then reacted as described in Example 36, Step 5 to provide [5-(4-bromo-2-chloro-phenyl)-3-methyl-isoxazol-4-yl]-carbamic acid (R)-1-(2-chloro-phenyl)-ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048902B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-f4f1e5bf6c354154a0785fa588ee10f6 |
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| Source note | uspto-grants-2011_11 |
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