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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506005Generated: November 3, 2026

Hydroxyamine hydrochloride → HCID 72295607, compound

https://huagongshe.com/reaction/506005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantHCID 59425473HCID 59425473—
ReactantHCID 59425954HCID 59425954—
SolventEthanolHCID 702—
ProductHCID 72295607HCID 7229560792%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 1-(1-ethyl-6-methoxy-1-H-indole-3-yl)ethanone (200 mg, 0.92 mmol), prepared from 1-ethyl-6-methoxy-1H-indole by the procedure described in example 1L, hydroxyamine hydrochloride (128 mg, 1.84 mmol), NaOAc (151 mg, 1.84 mmol) and EtOH (7 mL) is heated at 85° C. for 4 h. The reaction mixture is then partitioned between H2O and EtOAc. The organic phase is dried and concentrated in vacuo. Purification by column chromatography using EtOAc/CH2Cl2 (1/9) yields 1-(1-ethyl-6-methoxy-1-H-indole-3-yl)ethanone oxime as a white solid (189 mg, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781478B2
Source datasetuspto-grants-2010_08
ORD IDord-5bc8c8c5d3be4d2c8c95a205f097bf31
Source noteuspto-grants-2010_08