Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11397Generated: October 27, 2026

Iodoethane → N-(Benzensulfonyl)-5-chloro-2-ethylindole

https://huagongshe.com/reaction/11397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant5-Chloro-1-(phenylsulfonyl)indoleHCID 6472650—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductN-(Benzensulfonyl)-5-chloro-2-ethylindoleHCID 21974278—

Reaction Steps

t-BuLi (3.7 mL of 1.7 M solution in pentane) was added dropwise to a solution of N-(benzensulfonyl)-5-chloroindole (1) (J. Org. Chem. 1981, 46, 3859) (1.5 g, 5.14 mmol) in THF (35 mL) at −70° C., under a nitrogen atmosphere. The mixture was stirred for 15 min, allowed to warm to room temperature over 20 min, cooled to −70° C., and treated with a solution of ethyl iodide (0.84 mL, 10.5 mmol) in dry THF (5 mL). The mixture was stirred at −78° C. for 1 h, allowed to warm to room temperature, stirred for 2 h, poured into ice (15 g), and a saturated aqueous NH4Cl solution and then extracted with ether (3×20 mL). The combined organic extracts were washed with brine, dried (Na2SO4) and evaporated in vacuo to give a residue which was purified by flash chromatography (silica gel, cyclohexane/ethyl acetate, 8:2) and crystallization from ethylacetate/cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098233B2
Source datasetuspto-grants-2006_08
ORD IDord-25f95517642f49208b1291046c1ef585
Source noteuspto-grants-2006_08