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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071083Generated: November 2, 2026

Ethanol → HCID 44596115, compound

https://huagongshe.com/reaction/1071083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalyl chlorideHCID 65578—
Reactant6-FluoroindoleHCID 351278—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44596115HCID 44596115—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-fluoroindole (1.18 g, 8.56 mmol) in dry THF (65 mL) at 0° C. under argon was added (COCl)2 (0.93 mL, 10.7 mmol). The reaction mixture was stirred at 0° C. for 2 h and at rt for 15 h. The reaction mixture was cooled to 0° C. and EtOH (0.90 mL, 15.5 mmol) was added. The reaction mixture was stirred at rt for 24 h, then poured into cold satd NaHCO3. The mixture was extracted with EtOAc. The combined EtOAc extracts were washed with satd aq NaHCO3 and brine, dried, and evaporated to give the title compound: TLC Rf=0.48 (19:1 CH2Cl2/Me2CO); MS (ESI−) m/z 234.0; 1H NMR (CDCl3, 300 MHz) δ 10.95 (1H), 8.38 (1H), 8.31 (1H), 7.07 (1H), 4.37 (2H), 1.39 (3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903090B2
Source datasetuspto-grants-2005_06
ORD IDord-d48b5ca3d9554ccbbd38baa67770529d
Source noteuspto-grants-2005_06