Basic information Safety Supplier Related

4-(Chlorosulfonyl)-benzoic acid methyl ester

Basic information Safety Supplier Related

4-(Chlorosulfonyl)-benzoic acid methyl ester Basic information

Product Name:
4-(Chlorosulfonyl)-benzoic acid methyl ester
Synonyms:
  • methyl 4-(chlorosulfonyl)benzoate(SALTDATA: FREE)
  • 4-(Methoxycarbonyl)benzenesulfonyl chloride
  • 4-Carbomethoxybenzenesulfonyl chloride
  • Methyl p-(chlorosulfonyl)benzoate
  • p-(Carbomethoxy)benzenesulfonyl chloride
  • Benzoic acid, 4-(chlorosulfonyl)-, Methyl ester
  • METHYL 4-(CHLOROSULFONYL)BENZOATE(RS20013285)
  • Benzoic acid, 4-(chlorosulfonyl)-, methyl ester (9CI)
CAS:
69812-51-7
MF:
C8H7ClO4S
MW:
234.66
Product Categories:
  • SULFONYLHALIDE
Mol File:
69812-51-7.mol
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4-(Chlorosulfonyl)-benzoic acid methyl ester Chemical Properties

Melting point:
72-73℃
Boiling point:
126 °C(Press: 0.05 Torr)
Density 
1.431
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
color 
Faint to light orange
InChI
InChI=1S/C8H7ClO4S/c1-13-8(10)6-2-4-7(5-3-6)14(9,11)12/h2-5H,1H3
InChIKey
MOFQDKOKODUZPK-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC=C(S(Cl)(=O)=O)C=C1
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Safety Information

RIDADR 
3261
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2904990090
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4-(Chlorosulfonyl)-benzoic acid methyl ester Usage And Synthesis

Uses

4-(Chlorosulfonyl)-benzoic acid methyl ester can be used as an organic synthesis raw material for the preparation of other heterocyclic compounds.

Synthesis

67-56-1

7516-60-1

69812-51-7

General procedure for the synthesis of methyl 4-(chlorosulfonyl)benzoate from methanol and 4-(chlorosulfonyl)benzoyl chloride: 4-chlorosulfonylbenzoic acid (5 g, 23 mmol) was dissolved in dichloroethane (10 mL), thionyl chloride (20 mL) was added, and the reaction mixture was heated to 80 °C, and the reaction was maintained at this temperature for 2 hours. Upon completion of the reaction, the reaction mixture was concentrated by rotary evaporator to give a brown solid. The resulting solid was cooled in an ice bath for 5 min, followed by the slow addition of pre-cooled methanol (40 mL) at 0 °C with stirring, a process that lasted for 5 min. The reaction mixture was gradually warmed up to room temperature and stirring was continued for 10 minutes. Finally, ice-cold water (40 mL) was added, at which time a white solid precipitated, and the solid product was collected by filtration and dried under vacuum to afford pure methyl 4-(chlorosulfonyl)benzoate (4.5 g, 84% yield). The product was characterized by NMR (400 MHz, DMSO-d6): δ, ppm: 3.84 (s, 3H), 7.70 (d, 2H, J = 8.4Hz), 7.93 (d, 2H, J = 8.4Hz).

References

[1] Patent: WO2005/66126, 2005, A1. Location in patent: Page/Page column 73-74
[2] Patent: US9247759, 2016, B2. Location in patent: Page/Page column 144; 145
[3] Recueil des Travaux Chimiques des Pays-Bas, 1957, vol. 76, p. 129,138,145

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