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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTert-Butyl nitriteHCID 10906—
Reactant15-Crown-5HCID 36336—
ReactantMethyl 2-amino-4-methylbenzo[d]thiazole-5-carboxylateHCID 22390084—
CatalystCuprous chlorideHCID 62652—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-chloro-4-methylbenzo[d]thiazole-5-carboxylateHCID 2239008077.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908884B2
Source datasetuspto-grants-2005_06
ORD IDord-3aa97c414aa54f4ab25150730a167a30
Source noteuspto-grants-2005_06