methyl 3-chlorosulfonylbenzoate

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Products Intro: Product Name:Methyl 3-(chlorosulfonyl)benzoate
CAS:63555-50-0
Purity:98% Package:1kg
Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:Methyl 3-(Chlorosulfonyl)benzoate
CAS:63555-50-0
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:Methyl 3-(chlorosulfonyl)benzoate
CAS:63555-50-0
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Products Intro: CAS:63555-50-0
Purity:98% Package:g-Kg Remarks:White crystalline powder
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Products Intro: Product Name:Methyl 3-(Chlorosulfonyl)benzoate
CAS:63555-50-0
Purity:0.98 Package:25KG;5KG;1KG

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methyl 3-chlorosulfonylbenzoate Basic information
Product Name:methyl 3-chlorosulfonylbenzoate
Synonyms:methyl 3-chlorosulfonylbenzoate;3-(Methoxycarbonyl)benzenesulfonyl chloride;Methyl benzoate-3-sulfonyl chloride;3-(Methoxycarbonyl)benzenesulphonyl chloride;Benzoic acid,3-(chlorosulfonyl)-, Methyl ester
CAS:63555-50-0
MF:C8H7ClO4S
MW:234.66
EINECS:
Product Categories:Acids and Derivatives
Mol File:63555-50-0.mol
methyl 3-chlorosulfonylbenzoate Structure
methyl 3-chlorosulfonylbenzoate Chemical Properties
Boiling point 345.6±25.0 °C(Predicted)
density 1.431
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form powder
color light orange
InChIInChI=1S/C8H7ClO4S/c1-13-8(10)6-3-2-4-7(5-6)14(9,11)12/h2-5H,1H3
InChIKeySQIBNKUEUWGZBH-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=CC(S(Cl)(=O)=O)=C1
EPA Substance Registry SystemBenzoic acid, 3-(chlorosulfonyl)-, methyl ester (63555-50-0)
Safety Information
RIDADR 3261
TSCA TSCA listed
HazardClass IRRITANT
PackingGroup 
HS Code 2916399090
MSDS Information
methyl 3-chlorosulfonylbenzoate Usage And Synthesis
UsesMethyl 3-(chlorosulfonyl)benzoate
Synthesis
Methanol

67-56-1

3-(CHLOROSULFONYL)BENZOYL CHLORIDE

4052-92-0

methyl 3-chlorosulfonylbenzoate

63555-50-0

General procedure for the synthesis of methyl 3-(chlorosulfonyl)benzoate from methanol and 3-chlorosulfonylbenzoyl chloride: 3-(chlorosulfonyl)benzoic acid chloride (2.4 g) was dissolved in dichloromethane (20 mL) and cooled to 0 °C. Pyridine (791 mg) and methanol (320 mg) were added sequentially under stirring. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the solvent was removed by evaporation under reduced pressure. The residue was filtered and washed with a solvent mixture of ethyl acetate and isopropyl ether. The filtrate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography with hexane-ethyl acetate (9:1→4:1) as eluent to afford the target compound methyl 3-(chlorosulfonyl)benzoate (2.17 g, 92% yield) as colorless oil. The structure of the product was confirmed by 1H-NMR (CDCl3): δ 3.99 (3H, s), 7.74 (1H, t, J=8.1 Hz), 8.21-8.24 (1H, m), 8.39-8.43 (1H, m), 8.69-8.70 (1H, m).

References[1] Patent: EP1728793, 2006, A1. Location in patent: Page/Page column 127
[2] Patent: WO2006/36024, 2006, A1. Location in patent: Page/Page column 156
[3] Patent: EP2336107, 2015, B1. Location in patent: Paragraph 0296
[4] Recueil des Travaux Chimiques des Pays-Bas, 1921, vol. 40, p. 726
[5] Patent: WO2007/23186, 2007, A1. Location in patent: Page/Page column 49
methyl 3-chlorosulfonylbenzoate Preparation Products And Raw materials
Raw materialsMETHYL 3-AMINOBENZOATE-->sodium-compound-->Methanol-->3-(CHLOROSULFONYL)BENZOYL CHLORIDE-->Pyridine-->Dichloromethane
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