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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202362Generated: November 2, 2026

Benzothiazole → 1,3-Benzothiazole-4-sulfonyl chloride

https://huagongshe.com/reaction/2202362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantChlorosulfonic acidHCID 24638—
Product1,3-Benzothiazole-4-sulfonyl chlorideHCID 1495121217%

Reaction Steps

Benzo[d]thiazole (1 g, 7.45 mol) was added dropwise to chlorosulfonic acid (5.5 mmol) at 0° C. After the addition was complete, the mixture was stirred at room temperature for 0.5 h and then heated at 105° C. and stirred overnight. The resulting mixture was cooled to −10° C. and quenched by pouring on crushed ice slowly. The resulting mixture was extracted with EtOAc (100 mL×2). The combined organic phase was washed with brine, dried over anhy. Na2SO4 and concentrated in vacuo. Column chromatography (15% PE/EtOAc) afforded 218 mg of title compound. 1H NMR (CHLOROFORM-d) δ: 9.41 (s, 1H), 8.41 (dd, J=8.1, 1.0 Hz, 1H), 8.29 (dd, J=7.7, 1.1 Hz, 1H), 7.68 (t, J=7.9 Hz, 1H). LC-MS: m/z 234.7 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365545B2
Source datasetuspto-grants-2016_06
ORD IDord-c81afb7dd7cd414e9531edf8be8d51ab
Source noteuspto-grants-2016_06