HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071905Generated: October 26, 2026
Sodium Chloride → Methyl 2-chloro-4-methylbenzo[d]thiazole-5-carboxylate
https://huagongshe.com/reaction/1071905
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 15-Crown-5 | HCID 36336 | — |
| Reactant | Methyl 2-amino-4-methylbenzo[d]thiazole-5-carboxylate | HCID 22390084 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-chloro-4-methylbenzo[d]thiazole-5-carboxylate | HCID 22390080 | 77.3% |
Reaction Steps
A solution of 5 g (22.5 mmol) of methyl 2-amino-4-methyl-benzothiazole-5-carboxylate in 2 l of acetonitrile was admixed with 10 ml of water, 4.5 g (44.8 mmol) of copper(I) chloride, 6.6 g of sodium chloride (110 mmol) and 2 ml of 15-crown-5. A solution of 3 g (29 mmol) of tert-butyl nitrite was then added dropwise with stirring, the solution was heated at reflux for 15 h, the resulting precipitate was filtered off and the solution was concentrated under reduced pressure. The residue was then extracted three times with in each case 500 ml of ethyl acetate. To this end, the solvent was heated to boiling point and the solution was filtered whilst hot. The extracts were concentrated under reduced pressure. The residue was purified by trituration with n-hexane/diethyl ether. This gave 4.2 g (17.4 mmol, 77% yield) of methyl 2-chloro-4-methylbenzothiazole-5-carboxylate of m.p. 112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06908884B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-3aa97c414aa54f4ab25150730a167a30 |
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| Source note | uspto-grants-2005_06 |
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