HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449992Generated: October 25, 2026
Carbon Dioxide → 1,2-Benzisothiazole-3-carboxylic acid
https://huagongshe.com/reaction/449992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | 4-Chloro-3-nitrobenzoic acid | HCID 7320 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Benzothiazolamine, 4-chloro- | HCID 29872 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 1,2-Benzisothiazole-3-carboxylic acid | HCID 94512 | — |
| Product | 1,3-Benzothiazole-5-carboxylic acid | HCID 2735460 | — |
| Product | 1,3-Benzothiazole-4-carboxylic acid | HCID 20398548 | — |
Reaction Steps
The benzisoxazole-, benzisoxazole-, and benzothiazolecarboxylic acids were prepared using similar strategies outlined for the indazole acids. For example, ethyl 6-bromobenzisoxazole-3-carboxylate was prepared from 2,5-dibromonitrobenzene by reaction with diethyl malonate, saponification and decarboxylation, and reaction with isoamylnitrite. Ethyl benzisoxazole-3-carboxylate was obtained by hydrogenolysis of the 6-bromo derivative. 4-Benzothiazolecarboxylic acid was prepared from 2-amino-4-chloro-benzothiazole by reaction with isoamyl nitrite followed by metal-halogen exchange and trapping with carbon dioxide. 5-Benzothiazolecarboxylic acid was prepared from 4-chloro-3-nitrobenzoic acid by reaction with Na2S and sodium hydroxide followed by reduction with zinc in formic acid. 3-Benzisothiazolecarboxylic acid was prepared from thiophenol by reaction with oxalyl chloride and aluminum chloride followed by treatment with hydroxylamine, hydrogen peroxide, and sodium hydroxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486937B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-2d79172671204d0cb7d2bb9800e043fe |
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| Source note | uspto-grants-2013_07 |
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