Identification | More | [Name]
3-METHOXYBENZENESULFONYL CHLORIDE | [CAS]
10130-74-2 | [Synonyms]
3-METHOXYBENZENESULFONYL CHLORIDE 3-METHOXYBENZENESULPHONYL CHLORIDE AKOS BB-9459 BENZENESULFONYL CHLORIDE, 3-METHOXY- m-Anisolesulphonyl chloride m-Anisolesulfonylchloride 3-Methoxybenzenesulphonyl chloride 97% | [EINECS(EC#)]
628-640-1 | [Molecular Formula]
C7H7ClO3S | [MDL Number]
MFCD01318155 | [Molecular Weight]
206.65 | [MOL File]
10130-74-2.mol |
Chemical Properties | Back Directory | [Appearance]
Clear pale yellow to pale brownish liquid | [Boiling point ]
158-159°C 20mm | [density ]
1.460 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.5560(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
Liquid | [color ]
Clear pale yellow to pale brownish | [Sensitive ]
Moisture Sensitive | [BRN ]
2093871 | [CAS DataBase Reference]
10130-74-2(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
C,Xi | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . S39:Wear eye/face protection . S37:Wear suitable gloves . S36:Wear suitable protective clothing . | [RIDADR ]
UN 3265 8/PG 2
| [WGK Germany ]
3
| [Hazard Note ]
Corrosive/Moisture Sensitive | [HazardClass ]
8 | [PackingGroup ]
II | [HS Code ]
29093090 |
Hazard Information | Back Directory | [Chemical Properties]
Clear pale yellow to pale brownish liquid | [Uses]
3-Methoxybenzenesulfonyl chloride may be used to synthesize 3-(4-phenylpiperazin-1yl) sulfonyls and N-(1-(4-methoxybenzyl)-3-cyclopropyl-1Hpyrazol-5-yl)-3-methoxybenzenesulfonamide. | [Synthesis]
In another flask, a mixed solution of 450 mL of glacial acetic acid with 45 mL of water was saturated with sulfur dioxide gas at 25°C (about 180 g of sulfur dioxide was required). To this saturated solution, 20.4 g (0.12 mol) of copper(II) chloride was added and sulfur dioxide gas was passed again to saturation. A pre-prepared and cooled diazonium salt solution was added slowly and dropwise to the above stirred mixture in the range of 20-26 °C. There was a release of gas during the reaction, followed by a slow increase of the reaction temperature to 38°C. When the temperature started to drop naturally, external heating was applied to keep the mixture stirred at 50°C for 15 minutes. Upon completion of the reaction, the mixture was cooled to room temperature and quenched by pouring into 2 kg of ice water. The oily product in the reaction mixture was extracted with ether (2 x 1000 mL). The ether layers were combined and washed sequentially with 1N NaOH solution (2×1000 mL), 1N HCl solution (2×1000 mL), and saturated brine (1×1000 mL), then dried with anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to give 59.59 g of dark-colored oily crude product. The crude product was purified by silica gel column chromatography (silica gel dosage: 900 g) with dichloromethane/hexane (1:4, v/v) as eluent to give 43.52 g (43% yield) of 3-methoxybenzenesulfonyl chloride and 3.18 g of unidentified impurities. The products were analyzed by thin-layer chromatography (TLC) using silica gel plates with dichloromethane:hexane (1:1) as the unfolding agent, with an Rf value of 0.56 for the products and 0.41 for the impurities. | [References]
[1] Patent: US6342504, 2002, B1. Location in patent: Page column 124 |
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