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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736982Generated: October 29, 2026

Methyl 4-(Chlorosulfonyl)benzoate → HCID 58975020, compound

https://huagongshe.com/reaction/736982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(Chlorosulfonyl)benzoateHCID 4738388—
Reactant3-(propan-2-yl)-1H-indoleHCID 12534824—
ReactantWater ethylacetateHCID 22728543—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 58975020HCID 5897502051.1%

Reaction Steps

Add potassium tert butoxide 1.0 M (1.6 mL, 0.0016 mol) dropwise to a stirring solution of 3-isopropyl indole (0.217 g, 00136 mol) in dry DMF (20 mL) under N2 at ambient temperature. Stir the reaction mixture for 30 minutes and add portionwise 4-chlorosulfonyl benzoic acid methyl ester (0.328 g, 0.0014 mol). The light brown reaction mixture decolorizes immediately. Stir the resulting yellow solution overnight. Pour into a EtOAc—H2O mixture (100 to 300 mL). Separate the EtOAc and sequentially extract with H2O (3×250 mL), wash with brine, dry (MgSO4), filter and evaporate giving 0.38 g. Chromatograph on the ISCO using a gradient hexane-EtOAc (0-50%, 30 30 minutes) to give 0.249 g (51%) of the title compound as a waxy solid. Mass spectrum (m/e) (M+H) 358.1113. found (M+H) 358.1129.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595339B2
Source datasetuspto-grants-2009_09
ORD IDord-51075de71dd443a683313cac638ae469
Source noteuspto-grants-2009_09