Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243167Generated: November 1, 2026

Water → 5-allyloxy-1-benzenesulfonyl-1H-indole

https://huagongshe.com/reaction/2243167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
Reactant5-(prop-2-en-1-yloxy)-1H-indoleHCID 14239230—
SolventTetrahydrofuranHCID 8028—
Product5-allyloxy-1-benzenesulfonyl-1H-indoleHCID 6854937648.2%

Reaction Steps

To a slurry of 0.45 g (9.4 mmol) sodium hydride (50% dispersion in mineral oil) in 40 mL anhydrous THF was added 1.90 g 5-allyloxyindole. The slurry was stirred at room temperature for 15 min upon which time 1.14 mL (9 mmol) benzene sulfonyl chloride was added dropwise. The reaction was stirred at room temperature over three nights and then poured into water and extracted with ethyl acetate. The organic extracts were dried over MgSO4 and concentrated. The product solidified upon concentration and the crude material was triturated with diethyl ether to afford 1.36 g of 5-allyloxy-1-benzenesulfonyl-1H-indole as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674818B2
Source datasetuspto-grants-2010_03
ORD IDord-a5c1120043394832be0509a5cbce0f84
Source noteuspto-grants-2010_03