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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260478Generated: October 26, 2026

Sodium Sulfate → Ethyl 3-phenylsulfonyl-5-chloroindole-2-carboxylate

https://huagongshe.com/reaction/260478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactantethyl 5-chloro-3-(phenylthio)-1H-indole-2-carboxylateHCID 15035363—
SolventChloroformHCID 6212—
ProductEthyl 3-phenylsulfonyl-5-chloroindole-2-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527819
Source datasetuspto-grants-1996_06
ORD IDord-7dfdef450b614492b008d81f7e5aa352
Source noteuspto-grants-1996_06