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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5594Generated: October 27, 2026

Indole → 1-Phenyl-1H-indole

https://huagongshe.com/reaction/5594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantDimethylformamideHCID 6228—
ReactantBromobenzeneHCID 7961—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
Product1-Phenyl-1H-indoleHCID 18202920.2%

Reaction Steps

A mixture of 17.57 g (0.15 mole) of indole, 23.55 g (0.15 mole) of bromobenzene, 21 g of anhydrous potassium carbonate, 0.75 g of CuO, and 30 mL of DMF was stirred and heated under reflux for 43 hours. The cooled mixture was diluted with 200 mL of H2O and extracted with 150 mL of ether. The extract was washed with H2O (2×50 mL) and 50 mL of brine and dried over MgSO4. The oil was chromatographed on the solvent left 35.7 g of brown oil. The oil was chromatographed on a 1100 g column of silica gel. The column was eluted with 25% CH2Cl2 -Skellysolve B and 200 mL fractions were collected. The fractions were assayed by silica gel tlc (1×4") (25% CH2Cl2 -Skellysolve B). Fractions 15-22 were combined giving 5.86 g (20%) of 1-phenylindole as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245046
Source datasetuspto-grants-1993_09
ORD IDord-9e54ac87e6cd4333953c4b9787bd6f06
Source noteuspto-grants-1993_09