Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288258Generated: November 1, 2026

Water → (2s)-Glycidyl indol-4-yl ether

https://huagongshe.com/reaction/2288258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium fluorideHCID 25953—
Reactant1H-indol-4-olHCID 75421—
ReactantBenzenesulfonic acid, 3-nitro-, (2S)-2-oxiranylmethyl esterHCID 146490—
SolventDimethylformamideHCID 6228—
Product(2s)-Glycidyl indol-4-yl etherHCID 1094325494.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Hydroxyindole (3.0 g) was dissolved in DMF (10 ml) under nitrogen atmosphere and the solution was cooled to 0° C. Cesium fluoride (10.12 g) was added thereto and the mixture was stirred for 1 hour. Then (S)-glycidyl m-nitrobenzenesulfonate (5.84 g, 99.3% e.e.) was added thereto and the mixture was stirred for 30 hours at the same temperature. After the reaction, water was added to the mixture, the mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, condensed and the residue was subjected to silica gel chromatography (hexane/isopropyl alcohol; 20:1) to give 4.01 g of (S)-4-(2,3-epoxypropoxy)indole (yield 94.1%, optical purity 99.2% e.e.) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087512
Source datasetuspto-grants-2000_07
ORD IDord-4012f1f38a9b4b8c97a2facaa3a64e07
Source noteuspto-grants-2000_07