Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280821Generated: October 30, 2026

Water → 2-ethyl-4-hydroxy-1-(2-phenyl-phenylmethyl)-1H-indole

https://huagongshe.com/reaction/1280821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethyl benzenesulfinateHCID 2759784—
Reactant2-ethyl-1,5,6,7-tetrahydro-1-(2-phenyl-phenylmethyl)-4H-indol-4-oneHCID 18426120—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product2-ethyl-4-hydroxy-1-(2-phenyl-phenylmethyl)-1H-indoleHCID 1061620539.3%

Reaction Steps

2-Ethyl-1,5,6,7-tetrahydro-1-(2-phenyl-phenylmethyl)-4H-indol-4-one (2.17 g, 0.0066 mol) dissolved in 10 mL of tetrahydrofuran was added to a slurry of sodium hydride (0.58 g) in 3 mL of tetrahydrofuran and the mixture was stirred for 15 min at room temperature. Methyl benzene sulfinate (1.13 g) was added and the solution stirred overnight. The reaction mixture was poured into water, the pH adjusted to 6 with acetic acid and extracted with toluene. The organic layer was separated, washed with water and brine, dried with sodium sulfate, concentrated, taken up in toluene (80 mL) and heated at reflux for 1.5 h. After cooling, the mixture was concentrated, dissolved in ether (100 mL), washed with saturated sodium bicarbonate solution, dried over sodium sulfate, concentrated and purified by flash chromatography on silica eluting with 10:1 hexane/ethyl acetate to afford 0.85 g of subtitled material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451839B1
Source datasetuspto-grants-2002_09
ORD IDord-af647e2880be4ad7aa6afee1ec02e6bc
Source noteuspto-grants-2002_09