Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831856Generated: October 31, 2026

Indole → 1-Benzylindole

https://huagongshe.com/reaction/1831856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantEthyl AcetateHCID 8857—
ReactantDabcoHCID 9237—
ReactantDimethylacetamideHCID 31374—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
Product1-BenzylindoleHCID 9691380%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a mixture of indole (234 mg, 2.0 mmol), DBC (726 mg, 3.0 mmol), DABCO(67.2 mg, 0.6 mmol) and TBAC (556 mg, 2.0 mmol) is added DMA (4 mL). The resulting solution is heated at 135° C. for 2 h. The reaction mixture is cooled to RT and diluted with EtOAc (50 mL) and H2O (50 mL). The two layers are separated and the aqueous layer is back extracted with EtOAc (50 mL). The combined organic layers are washed with brine and dried over anhydrous Na2S04. The mixture is filtered and concentrated under vacuum. The crude residue is purified with Biotage Flash Chromatography unit on 40s cartridge eluting with hexane:CH2Cl2=19:1 solvent mixture to afford 1-benzylindole (about 331.2 mg, 80%) as a white solid: mp 43° C.; 1H NMR (CDCl3) δ 7.38 (m, 9H), 6.73 (d, 1H), 5.48 (s, 2H); 13C NMR (CDCl3) δ 137.5, 136.3, 128.7, 128.2, 127.6, 126.7, 121.6, 120.9, 119.5, 109.7, 101.6, 50.0; MS m/z 207.1043 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067676B2
Source datasetuspto-grants-2006_06
ORD IDord-7793c8849084467cb9dff3241b8473fd
Source noteuspto-grants-2006_06