4-(Chlorosulfonyl)-benzoic acid methyl ester
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
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
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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4-(Chlorosulfonyl)-benzoic acid methyl ester(69812-51-7)Related Product Information
- Phthalic acid
- 4-(CHLOROSULFONYL)BENZOIC ACID
- BUTTPARK 88\11-08
- BUTYL 4-(CHLOROSULFONYL)BENZOATE
- 4-CHLOROSULFONYL-BENZOIC ACID ETHYL ESTER
- propyl 3-bromo-4-(chlorosulfonyl)benzoate
- butyl 3-bromo-4-(chlorosulfonyl)benzoate
- methyl 4-(chlorosulfonyl)-3-nitrobenzoate
- 4-(Chlorosulfonyl)-benzoic acid methyl ester
- BUTTPARK 147\11-86
- ethyl 3-bromo-4-(chlorosulfonyl)benzoate
- PROPYL 4-(CHLOROSULFONYL)BENZOATE
- ISOPROPYL 4-(CHLOROSULFONYL)BENZOATE