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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684830Generated: November 2, 2026

Acetone → 2-(4'-Nitrophenyl)-6-methylsulfoxy benzothiazole

https://huagongshe.com/reaction/1684830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium CarbonateHCID 11430—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant6-Benzothiazolol, 2-(4-nitrophenyl)-HCID 10890999—
Product2-(4'-Nitrophenyl)-6-methylsulfoxy benzothiazoleHCID 6726400468%

Reaction Steps

To a solution of 2-(4′-nitrophenyl)-6-hydroxy benzothiazole (50 mg, 0.18 mmol) dissolved in acetone (7 mL, anhydrous) was added K2CO3 (100 mg, 0.72 mmol, powdered) and MsCl (200 ul). After stirring for 2 hrs, the reaction mixture was filtered. The filtrate was concentrated and the residue was purified by flash column (silica gel, hexane:ethyl acetate=4:1) to give 2-(4-nitrophenyl)-6-methylsulfoxy benzothiazole (44 mg, 68%) as pale yellow solid. 1HNMR (30 MHz, acetone-d6) δ (ppm): 8.50-8.40 (m, 4H), 8.29 (d, J=2.3 Hz, 1H), 8.23 (d, J=8.9 Hz, 1H), 7.61 (dd, J1=2.3 Hz, J2=8.9 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08147798B2
Source datasetuspto-grants-2012_04
ORD IDord-b0440208bb064fc9abb13d3d1bdff989
Source noteuspto-grants-2012_04