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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127268Generated: October 27, 2026

Triphenylphosphine → 3-(2-bromoethyl)-6-methoxy-1H-indole

https://huagongshe.com/reaction/127268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant2-(6-Methoxy-1h-indol-3-yl)ethanolHCID 20485101—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product3-(2-bromoethyl)-6-methoxy-1H-indoleHCID 11736899—

Reaction Steps

To a mechanically stirred mixture of 18.3 g (69.7 mmol) triphenylphosphine and 200 ml acetonitrile, 11.15 g (69.7 mmol) bromine is added dropwise over 20 minutes. The mixture is stirred 20 minutes at 0° and the ice bath is removed. A solution of 12.1 g (63.4 mmol) 6-methoxy-3-(2-hydroxyethyl)indole in 60 ml acetonitrile is added over 30 minutes. After stirring 2 hours at room temperature the mixture is diluted with 250 ml diethyl ether. The liquid is decanted from precipitated tar. The residue is washed with an additional 250 ml diethyl ether. The volume of the ethereal extracts is reduced to about 60 ml and the solution is filtered through 75 g silica gel with diethyl ether. The solvent is removed to yield 6-methoxy-3-(2-bromoethyl)indole, 4.1 g, yellow waxy solid, mp 98°-101°, which turns green on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255432
Source datasetuspto-grants-1981_03
ORD IDord-1af3e70acf944dccbf459d1421d22719
Source noteuspto-grants-1981_03