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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179288Generated: October 31, 2026

Indole → HCID 9942622, compound

https://huagongshe.com/reaction/2179288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantDodecaneHCID 8182—
ReactantAmmonium HydroxideHCID 14923—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantBenzene, 1-bromo-3,5-dimethyl-HCID 136357—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDiethylsalicylamideHCID 88006—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 9942622HCID 994262289%

Reaction Conditions

Temperature100 °C

Reaction Steps

CuI (10 mg, 0.05 mmol), N,N-diethylsalicylamide (10 mg, 0.05 mmol), indole (176 mg, 1.5 mmol) and K3PO4 (425 mg, 2.0 mmol) were put into a screw-capped test tube with a Teflon-lined septum. The tube was then evacuated and backfilled with argon (3 cycles). 5-Bromo-m-xylene (136 μL, 1.0 mmol) was added by a syringe. The reaction mixture was stirred at 100° C. for 20 h. The reaction mixture was allowed to reach room temperature. Ethyl acetate (˜2 mL), water (˜10 mL), ammonium hydroxide (˜0.5 mL) and dodecane (227 μL) were added. The organic phase was analyzed by GC or GC-MS. The reaction mixture was further extracted by ethyl acetate (4×10 mL). The combined organic phases were washed with brine and dried over Na2SO4. Solvent was removed in vacuo and the yellow residue was purified by column chromatography on silica gel using hexane/ethyl acetate (10:1) as eluent to afford the desired product as a brown solid (196 mg, 89% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067955B2
Source datasetuspto-grants-2015_06
ORD IDord-48be51aae2ea45ef81b57823ddd666c1
Source noteuspto-grants-2015_06