Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221231Generated: November 1, 2026

Ethanol → ethyl [1-benzyl-6-(3-chlorophenyl)-1H-indol-3-yl](oxo)acetate

https://huagongshe.com/reaction/2221231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalyl chlorideHCID 65578—
Reactant1-benzyl-6-(3-chlorophenyl)-1H-indoleHCID 22032942—
Productethyl [1-benzyl-6-(3-chlorophenyl)-1H-indol-3-yl](oxo)acetateHCID 22032985—

Reaction Steps

Ethyl [1-benzyl-6-(3-chlorophenyl)-1H-indol-3-yl](oxo)acetate was prepared from 1-benzyl-6-(3-chlorophenyl)-1H-indole (0.591 g, 1.86 mmol), oxalyl chloride (0.49 mL, 5.6 mmol), and ethanol (2 mL) following the procedure described in Step 3 of Example 1. Purification by flash chromatography using 5-100% ethyl acetate in hexane as an eluant yielded the title compound as a hard reddish gum (0.520 g, 67%). Mass spectrum (+ESI, [M+H]+) m/z 418; 1HNMR (500 MHz, DMSO-d6): δ 8.7 (s, 1H), 8.25 (d, 1H, J=8.2 Hz), 8.0 (s, 1H), 7.8 (s, 1H), 7.65-7.0 (m, 2H), 7.5 (t, 1H, J=7.9 Hz), 7.4 (d, 1H, J=0.92 Hz), 7.35-7.4 (m, 4H), 7.25-7.3 (m, 1H), 5.7 (s, 2H), 4.35 (q, 2H, J=7.1 Hz), and 1.35 ppm (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368471B2
Source datasetuspto-grants-2008_05
ORD IDord-006d22408a7543bb9965e3e55bc98415
Source noteuspto-grants-2008_05