HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfate → Ethyl 3-phenylsulfonyl-5-chloroindole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | ethyl 5-chloro-3-(phenylthio)-1H-indole-2-carboxylate | HCID 15035363 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 3-phenylsulfonyl-5-chloroindole-2-carboxylate | HCID 22401503 | — |
Reaction Steps
Ethyl 3-phenylthio-5-chloroindole-2-carboxylate (642 mg, 1.94 mmol) was dissolved in chloroform (35 mL) and a dried (Na2SO4) solution of m-chloroperoxybenzoic acid (55% pure, 1.30 g, 4.1 mmol) in chloroform (20 mL) was added dropwise. The progress of the oxidation was monitored by tlc until complete. After 5 hours, the reaction was diluted with chloroform and some methanol and the solution washed with aq. NaHCO3 and aq. Na2CO3. The dried (Na2SO4) organic layer was filtered through a pad of charcoal and the solvents removed under reduced pressure. The residue was triturated with diethyl ether to yield the product. Crystallization from methylene chloride and diethyl ether gave analytically pure material, mp 201°-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05527819 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-7dfdef450b614492b008d81f7e5aa352 |
| Source note | uspto-grants-1996_06 |