HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2-(4'-Nitrophenyl)-6-methylsulfoxy benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 6-Benzothiazolol, 2-(4-nitrophenyl)- | HCID 10890999 | — |
| Product | 2-(4'-Nitrophenyl)-6-methylsulfoxy benzothiazole | HCID 67264004 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08147798B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-b0440208bb064fc9abb13d3d1bdff989 |
| Source note | uspto-grants-2012_04 |