Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethylsulfamoyl chloride | HCID 11040810 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54105243 | HCID 54105243 | 71% |
Reaction Steps
A solution of 18.8 g (0.2 mole) of phenol and 38.4 g (0.27 mole) of ethylaminosulfonyl chloride (prepared using procedure of Example 2, pt. a) in 150 ml of toluene was stirred and heated at reflux for 16 hr. The solution was cooled and then treated with 250 ml of a 20% sodium bicarbonate solution. The layers were separated and the organic layer was washed successively with 250 ml of a 20% sodium bicarbonate solution, two 300-ml portions of water and dried (magnesium sulfate). The solvent was evaporated under reduced pressure and the oily residue was purified by chromatography (4.5×105 cm glass column; 550 g of silica gel; ethyl acetate-hexanes, 1:16). Fractions containing the product were combined and the solvents evaporated under reduced pressure to give 28.5 g (71%) of the title compound as a colorless liquid. Elemental analysis suggested that the product contained water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05025031 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-ecbed0833ab74b2e879cf84ab5f4e5db |
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| Source note | uspto-grants-1991_06 |
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