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| (4-Methylphenyl)sulfonyl acetate Basic information |
Product Name: | (4-Methylphenyl)sulfonyl acetate | Synonyms: | Acetic Acid, Anhydride With P-Toluenesulfonic Acid;Acetic P-Toluenesulfonic Anhydride;(4-METHYLPHENYL)SULFONYL ACETATE;UOAJUPONZOXFNX-UHFFFAOYSA-N;acetyl p-toluenesulfonate;Acetic acid, anhydride with 4-methylbenzenesulfonic acid;(4-Methylbenzene)sulfonyl Acetate | CAS: | 26908-82-7 | MF: | C9H10O4S | MW: | 214.24 | EINECS: | | Product Categories: | | Mol File: | 26908-82-7.mol | |
| (4-Methylphenyl)sulfonyl acetate Chemical Properties |
Melting point | 54-56 °C | Boiling point | 325.7±35.0 °C(Predicted) | density | 1.279±0.06 g/cm3(Predicted) | solubility | sol acetonitrile, dichloromethane, toluene | form | crystals | color | colorless |
| (4-Methylphenyl)sulfonyl acetate Usage And Synthesis |
Preparation | (4-Methylphenyl)sulfonyl acetate prepared from Acetyl Chloride and
p-Toluenesulfonic Acid[1]. | storage | the solid is readily hydrolyzed, so it must be protected from contact
with moisture; thermal decomposition is also possible. | Purification Methods | The most likely impurity is p-toluenesulfonic acid (could be up to 10%). This can be removed by dissolving it in dry Et2O and cooling until the anhydride crystallises out. It decomposes on heating; below ~130o it gives the disulfonic anhydride and above ~130o polymers are formed, but it can be distilled in a vacuum if it is free of acid. It is used for cleaving ethers [Prep, IR, NMR: Karger & Mazur J Org Chem 36 528, Karger & Mazur J Org Chem 36 532 1971]. [Beilstein 11 III 255.] | References |
[1]. (a) Karger, M. H.; Mazur, Y. JOC 1971, 36, 528. (b) Lin, J. S.; Sleezer, P. D. U.S. Patent 4 219 495, 1980.
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| (4-Methylphenyl)sulfonyl acetate Preparation Products And Raw materials |
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