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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913615Generated: October 30, 2026

Water → 5-[(Phenylmethyl)oxy]-1-(phenylsulfonyl)-2-propyl-1H-indole

https://huagongshe.com/reaction/913615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-IodopropaneHCID 33643—
Reactant5-(Phenylmethoxy)-1-phenylsulfonylindoleHCID 11824624—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-[(Phenylmethyl)oxy]-1-(phenylsulfonyl)-2-propyl-1H-indoleHCID 57800103—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution a −78° C. cooled (dry ice/acetone bath) of 5-[(phenylmethyl)oxy]-1-(phenylsulfonyl)-1H-indole (1.1 g, 0.003 mol) in THF (anhydrous, 10 mL) was added n-butyllithium (2.3 mL of a 1.6 M solution in hexanes) dropwise. The mixture was then warmed to −10° C. over 30 min and then cooled to −78° C. and 1-iodopropane (1.5 eq., 0.005 mol, 0.77 g) was added dropwise. The mixture was warmed to rt over 1 h and then stirred at rt for 20 min. Water (10 mL) and EtOAc (100 mL) was added. The organic layer was separated, dried (MgSO4), and concentrated. Purification via semipreparative reverse-phase HPLC provided the desired product: MS (ES) m/z 406 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026262B2
Source datasetuspto-grants-2011_09
ORD IDord-dbcbbdaca0204516a6b531f94e2395cf
Source noteuspto-grants-2011_09