Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370411Generated: November 2, 2026

Ethanol → HCID 12230410, compound

https://huagongshe.com/reaction/1370411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalyl chlorideHCID 65578—
Reactant4-ChloroindoleHCID 91345—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12230410HCID 12230410—

Reaction Steps

To a solution of 4-chloroindole (5.00 g, 33.0 mmol) in dry THF (0.2 L), at 0° C. under argon was added (COCl)2 (3.6 mL, 40.4 mmol). The reaction mixture was stirred overnight while warming to rt, cooled to 0° C., and EtOH (4 mL, 69 mmol) was added. The reaction mixture was stirred at rt overnight, then partitioned between cold 0.2 M aq HCl and EtOAc. The aqueous layer was separated and re-extracted with EtOAc. The EtOAc extracts were washed with saturated aqueous NaHCO3 and brine. The extracts were dried, filtered, and concentrated to give a solid. The solid was purified by silica chromatography to give the title compound: TLC Rf=0.40 (19:1 CH2Cl2/Me2CO); MS (ESI+) m/z 274.0; 1H NMR (300 MHz, CDCl3) δ 9.22 (1H), 8.26 (1H), 7.36 (1H), 7.31 (1H), 7.22 (1H), 4.71 (2H), 1.41 (3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583135B2
Source datasetuspto-grants-2003_06
ORD IDord-a3e9188dbaac4446b1acc83b5d6a0d8a
Source noteuspto-grants-2003_06