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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23412Generated: October 26, 2026

1,1-Dichloroethane → 5-chloro-1H-indole-3-sulfonic acid

https://huagongshe.com/reaction/23412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
ReactantTrimethylsilyl chlorosulphateHCID 78059—
Reactant7-chloro-1H-indoleHCID 104644—
Product5-chloro-1H-indole-3-sulfonic acidHCID 22574052—

Reaction Conditions

Temperature-10 °C

Reaction Steps

7-Chloroindole (1.51 g, 10 mmole) was dissolved in 2 ml dichloroethane and cooled under nitrogen to −10° C. in an ice-salt-acetone bath. Trimethylsilylchlorosulfonate (1.89 g, 1.6 ml, 10 mmole) was slowly added with stirring. Upon termination of the addition, the reaction was allowed to warm to room temperature and stirred for 30 min at this temperature. The dark red solution was evaporated to dryness and the solvent was replaced with 50 ml ethyl acetate. Methanol (5 ml) was added and the solvents were removed and the residue thoroughly dried to afford the crude 5-chloro-1H-indole-3-sulfonic acid as a red oil. Step 2 7-Chloro-1H-indole-3-sulfonic acid dimethylamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852726B2
Source datasetuspto-grants-2005_02
ORD IDord-70c1fae9fcc645429cb95f1019463575
Source noteuspto-grants-2005_02