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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620121Generated: October 29, 2026

Hydrochloric Acid → 2-Methyl-7-chlorosulfonylbenzothiazole

https://huagongshe.com/reaction/620121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
Reactant2-Methylbenzo[d]thiazol-7-amineHCID 13824430—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Methyl-7-chlorosulfonylbenzothiazoleHCID 13824431—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 8 g of the product from Example 7 in 20 mL of concentrated hydrochloric acid was cooled to 0° C. and treated with a solution of 3.7 g sodium nitrite in 6 mL of water. After completion of the addition, the mixture was stirred at 0°-5° C. for about 15 minutes. This diazonium salt solution was then added all at once to a mixture of liquid sulfur dioxide, 2 g of cupric chloride dihydrate, and 4 mL water in 39 mL of glacial acetic acid at about 10° C.; vigorous gas evolution ensued. This reaction mixture was stirred at room temperature for another 4 hours, and was then poured into 190 mL ice-water. The resulting precipitate was collected by filtration, washed with water, and dried to give 9.2 g of 2-methyl-7-chlorosulfonylbenzothiazole as a yellow powder, m.p. 93°-97° C., dec; IR(KBr): 1380, 1175, 800, 770, 720 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820332
Source datasetuspto-grants-1989_04
ORD IDord-23f8e17df7ae4cdfab839f0826cce913
Source noteuspto-grants-1989_04