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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981981Generated: October 30, 2026

Water → HCID 14956369, compound

https://huagongshe.com/reaction/981981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10042215HCID 10042215—
SolventDimethylformamideHCID 6228—
ProductHCID 14956369HCID 1495636970.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2.8 g (0.0085 mol) of 1-methyl-2-isopropyl-(4-hydroxy-benzenesulphonyl)indole in 100 ml of N,N-dimethyl formamide were added 14 g of anhydrous and crushed potassium carbonate. After that 6.8 g (0.037 mol) of 1,3-dibromopropane were added and the medium was heated at 100° C. for 0.5 hour. The mixture was poured into water, extracted with ethyl ether and the ethereal fraction was washed with water, dried on anhydrous sodium sulphate, filtered and evaporated to obtain 2.7 g of 1-methyl-3-[4-(3-bromo-propoxy)benzenesulphonyl]-2-isopropyl-indole (yield: 69%). This crude bromopropoxy derivative was dissolved in 60 ml of dimethylsulphoxide and 2.2 g (0.03 mol) of tert-butylamine were added. The medium was then stirred at room-temperature for 48 hours, poured into water and extracted with ethyl ether. The ethereal solution was then washed with water, dried on anhydrous sodium sulphate, filtered and evaporated. The crude product so obtained (2.3 g) was then purified by chromatography on a silica column (solvent:methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994474
Source datasetuspto-grants-1991_02
ORD IDord-69d19161565846ba8798498e2803f210
Source noteuspto-grants-1991_02